K Number
K093849
Manufacturer
Date Cleared
2010-01-19

(34 days)

Product Code
Regulation Number
892.1550
Reference & Predicate Devices
Predicate For
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use

The ACCUVIX V10 system and transducers are intended for diagnostic ultrasound imaging and fluid analysis of the human body. The clinical applications include: General, abdomen, obstetrics, gynecology, vascular, extremity, pediatric, cardiac, breast, urology, neonatal cephalic, trans-esophageal, intraoperative and etc.

Device Description

The ACCUVIX V10 is a general purpose, mobile, software controlled, diagnostic ultrasound system. Its function is to acquire ultrasound data and to display the data as 2D mode, M mode, Color Doppler mode, Power Doppler mode, PW Spectral Doppler, CW Spectral Doppler mode, and Tissue Doppler Image mode on the LCD display. It also provides the 3D/4D imaging mode using the 3D/4D probe in the Mechanical scan mode. The ACCUVIX V10 has real time acoustic output display with two basic indices, a mechanical index and a thermal index, which are both automatically displayed. The system also provides for the measurement of anatomical structures and for analysis packages that provide information used for clinical diagnostic purposes by competent health care professionals.

AI/ML Overview

Here's a breakdown of the acceptance criteria and study information for the ACCUVIX V10 Diagnostic Ultrasound System, based on the provided text:

Important Note: The provided document is a 510(k) Premarket Notification summary for substantial equivalence. It does not contain detailed information about a "study that proves the device meets the acceptance criteria" in the way one might expect for a clinical trial validating an AI algorithm. Instead, it describes how the device meets safety and performance standards and is substantially equivalent to previously cleared predicate devices. Therefore, the "acceptance criteria" here refer to regulatory and safety standards, and "device performance" relates to its intended uses and modes of operation, which are compared to the predicate devices. There is no information about AI-specific validation studies, as this device predates such common regulations.


Acceptance Criteria and Reported Device Performance

The acceptance criteria for the ACCUVIX V10 are based on its compliance with established safety standards and its substantial equivalence to predicate devices, particularly regarding its intended uses and modes of operation. The device performance is deemed acceptable if it meets these existing standards and offers functionalities comparable to or improved over the predicate devices.

Table 1: Acceptance Criteria (Regulatory Standards) and Reported Device Performance

Acceptance Criterion (Standard)Reported Device Performance
Safety Requirements for Medical Equipment:The ACCUVIX V10 has been designed to meet all listed product safety standards.
- UL 60601-1(Compliance implied by statement)
- CSA C22.2 No. 601.1(Compliance implied by statement)
- IEC60601-2-37 (Diagnostic Ultrasound Safety Standards)(Compliance implied by statement)
- EN/IEC60601-1(Compliance implied by statement)
- EN/IEC60601-1-2 (EMC requirements)(Compliance implied by statement)
Acoustic Output Standards:The system provides real-time acoustic output display with Mechanical Index (MI) and Thermal Index (TI), displayed automatically.
- NEMA UD-2 (Acoustic Output Measurement Standard)(Compliance implied by statement, system measures and displays outputs)
- NEMA UD-3 (Standard for Real Time Display of Thermal and Mechanical Acoustic Output Indices)(Compliance implied by statement, MI and TI are automatically displayed)
- IEC 61157 (Declaration of the acoustic output)(Compliance implied by statement)
Biocompatibility:
- ISO10993-1(Compliance implied by statement)
Intended Uses and Technological Characteristics (Substantial Equivalence):The device is substantially equivalent to K070813 (ACCUVIX V10 Diagnostic Ultrasound System) and K092159 (ACCUVIX V20 Diagnostic Ultrasound System). It acquires ultrasound data and displays it in 2D, M, Color Doppler, Power Doppler, PW Spectral Doppler, CW Spectral Doppler, and Tissue Doppler Image modes, including 3D/4D imaging. It provides measurement and analysis packages for clinical diagnostic purposes. It also supports various transducers and clinical applications (e.g., General, Abdomen, Obstetrics, Gynecology, Vascular, Cardiac, Breast, Pediatric). New indications for certain transducers are highlighted as "N," while "P" denotes previously cleared indications by predicate devices.

Study Information (Based on the 510(k) Summary)

As this is a 510(k) Pre-Market Notification for a diagnostic ultrasound system (filed in 2009), the "study" referred to is a demonstration of substantial equivalence to legally marketed predicate devices, rather than a clinical trial validating a new AI algorithm's performance against a ground truth.

There is no information in the provided document for the following points, as these types of studies and details are typically associated with performance validation of novel AI/ML devices, which is not the nature of this submission:

  1. Sample sizes used for the test set and the data provenance (e.g., country of origin of the data, retrospective or prospective): Not applicable for a 510(k) substantial equivalence submission for an ultrasound system. The demonstration of equivalence relies on device specifications, technical characteristics, and safety standards.
  2. Number of experts used to establish the ground truth for the test set and the qualifications of those experts: Not applicable.
  3. Adjudication method (e.g., 2+1, 3+1, none) for the test set: Not applicable.
  4. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance: Not applicable. This document is for a general diagnostic ultrasound system, not an AI-powered diagnostic tool requiring human-in-the-loop performance studies as understood today.
  5. If a standalone (i.e., algorithm only without human-in-the-loop performance) was done: Not applicable.
  6. The type of ground truth used (expert consensus, pathology, outcomes data, etc.): Not applicable.
  7. The sample size for the training set: Not applicable.
  8. How the ground truth for the training set was established: Not applicable.

Summary of "Study" in this Context:

The "study" or justification for approval in this 510(k) is the demonstration that the ACCUVIX V10 Diagnostic Ultrasound System is substantially equivalent to the following predicate devices:

  • K070813, ACCUVIX V10 Diagnostic Ultrasound System
  • K092159, ACCUVIX V20 Diagnostic Ultrasound System

Substantial equivalence is established by showing that the device has the same intended use and similar technological characteristics as the predicates, or if there are differences, that these differences do not raise new questions of safety and effectiveness. The document extensively lists safety standards the device meets and its various modes of operation and clinical applications, comparing them to what was previously cleared in the predicate devices. The presence of 'P' (previously cleared) and 'N' (new indication) for various transducers and clinical applications illustrates this comparison to the predicate devices.

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K093849

510(k) Premarket Notification

JAN 1 9 2010

ACCUVIX V10 Diagnostic Uitrasound System.

510(K) SUMMARY OF SAFETY AND EFFECTIVENESS

This summary of safety and effectiveness is provided as part of this Premarket Notification in compliance with 21 CFR, Part 807, Subpart E, Section 807.92.

1. Submitter's Information: 21 CFR 807.92(a)(1)

MEDISON CO., LTD. 1003, Daechi-dong, Gangnam-gu, Seoul 135-280, Korea

Contact Person:

Mr. Kyung-Am, Shim Regulatory Affairs Manager

Telephone:82.2.2194.1381
Facsimile:82.2.2194.1399
Email:kashim@medison.com

Data Prepared: September 7, 2009

2. Name of the device:

Common/Usual Name:

Diagnostic Ultrasound System and Accessories

Proprietary Name:

ACCUVIX V10 Diagnostic Ultrasound System

Classification Names:FR NumberProduct Code
Ultrasonic Pulsed Doppler Imaging System892.1550IYN
Ultrasound Pulsed Echo Imaging System892.1560IYO
Diagnostic Ultrasound Transducer892.1570ITX

3. Identification of the predicate or legally marketed device:

K070813, ACCUVIX V10 Diagnostic Ultrasound System K092159, ACCUVIX V20 Diagnostic Ultrasound System

4. Device Description:

The ACCUVIX V10 is a general purpose, mobile, software controlled, diagnostic ultrasound system. Its function is to acquire ultrasound data and to display the data as 2D mode, M mode, Color Doppler mode, Power Doppler mode, PW Spectral Doppler, CW Spectral Doppler mode, and Tissue Doppler Image mode on the LCD display. It also provides the 3D/4D imaging mode using the 3D/4D probe in the Mechanical scan mode.

The ACCUVIX V10 has real time acoustic output display with two basic indices, a

ATTACHMENT 1(b)

{1}------------------------------------------------

510(k) Premarket Notification

mechanical index and a thermal index, which are both automatically displayed. The system also provides for the measurement of anatomical structures and for analysis packages that provide information used for clinical diagnostic purposes by competent health care professionals.

The ACCUVIX V10 has been designed to meet the following product safety standards:

  • UL 60601-1, Safety requirements for Medical Equipment
  • CSA C22.2 No. 601.1, Safety requirements for Medical Equipment
  • IEC60601-2-37, Diagnostic Ultrasound Safety Standards
  • EN/IEC60601-1, Safety requirements for Medical Equipment
  • EN/IEC60601-1-2, EMC requirements for Medical Equipment
  • NEMA UD-2, Acoustic Output Measurement Standard for Diagnostic Ultrasound Equipment
  • NEMA UD-3, Standard for Real Time Display of Thermal and Mechanical Acoustic Output Indices on Diagnostic Ultrasound Equipment
  • IEC 61157, Declaration of the acoustic output
  • ISO10993-1, Biocompatibility

5. Intended Uses:

The ACCUVIX V10 system and transducers are intended for diagnostic ultrasound imaging and fluid analysis of the human body.

The clinical applications include:

General, abdomen, obstetrics, gynecology, vascular, extremity, pediatric, cardiac, breast, urology, neonatal cephalic, trans-esophageal, intraoperative and etc.

6. Technological Characteristics:

The ACCUVIX V10 is substantially equivalent to the ACCUVIX V10 Diagnostic Ultrasound System, cleared via K070813, and the ACCUVIX V20 Diagnostic Ultrasound System, cleared via K092159. All systems transmit ultrasonic energy into patients, then perform post processing of received echoes to generate on-screen display of anatomic structures and fluid flow within the body. All system allow for specialized measurements of structures and flow, and calculations.

END of 510(K) Summary

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

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Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized image of an eagle with its wings spread, facing to the left.

Food and Drug Administration 10903 New Hampshire Avenue Document Mail Center - WO66-G609 Silver Spring, MD 20993-0002

JAN 1 9 2010

Medison Co., Ltd. % Mr. Mark Job Responsible Third Party Official Regulatory Technology Services LLC 1394 25th Street NW BUFFALO MN 55313

Re: K093849

Trade/Device Name: ACCUVIX V10 Diagnostic Ultrasound System Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Regulatory Class: II Product Code: IYN, IYO, and ITX Dated: January 7, 2010 Received: January 8, 2010

Dear Mr. Job:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.

This determination of substantial equivalence applies to the following transducers intended for use with the ACCUVIX V10 Diagnostic Ultrasound System, as described in your premarket notification:

Transducer Model Number
3D2-6ETC2-61CNER4-9ES
3D4-8ETC3-71MNEV4-9ES
3D4-9ESC4-9/10EDL4-7EL
3D5-9EKEC4-9ISL5-12/50EP
V6-12ER4-9/10EDL5-13IS
C2-5ELEV4-9/10EDL6-12IS

{3}------------------------------------------------

L7-16ISMPT4-7P3-8CA
L8-15ISP2-4ACCW 2.0
LS5-13P2-4BACW 4.0
LT4-7P3-5AC

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807): labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

This letter will allow you to begin marketing your device as described in your premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus permits your device to proceed to market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to

http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

If you have any questions regarding the content of this letter, please contact Andrew Kang at (301) 796-6544.

Sincerely yours,

Donald J. St.Pierre Acting Director Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety Center for Devices and Radiological Health

Enclosure(s)

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… ﺃﺭ

..............................................................................................................................................................................

DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE STATEMENT

Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal ( See Note 3 )
Abdominal
Intra-operative ( See Note 6 )
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
PediatricP
Small Organ ( See Note 5 )
Neonatal Cephalic
Adult CephalicP
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph.(non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac AdultP
CardiacCardiac PediatricP
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vesselP
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E
Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD
Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
Note 6: Abdominal organs and peripheral vessel
Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D imaging
Note 9: Panoramic imaging.

Concurrence of CDRH, Office of Device Evaluation (ODE) (OIVD)
Prescription Use (Per 21 CFR 801.109)510(k) Number K093849

"

:

.

{5}------------------------------------------------


DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE STATEMENT

510(k) No.:K093849
Device Name:CW 2.0 for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult CephalicP
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac AdultP
Cardiac PediatricP
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vesselP
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: BM, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler/M, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

signature

Concurrence of CDRH, Callion and Prescription Use (Per 21 CFR 801.109)

510(k) Number: K093849

{6}------------------------------------------------

510(k) No.:
Device Name:1

Ko 93849 P3-8CA for use with ACCUVIX V10

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
AbdominalPPPPPNote 1Note 4, 7
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult CephalicPPPPPNote 1Note 4, 7
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac AdultPPPPPNote 1Note 4, 7
CardiacCardiac PediatricPPPPPNote 1Note 4, 7
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared under K092159; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: BM, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients,

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

S.L.R.

Concurrence of CDRH, Oblisa of Dougles Forman Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{7}------------------------------------------------

510(k) No.:K093849
Device Name:P3-5AC for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
AbdominalPPPPPNote 1Note 4, 7
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal ImagingLaparoscopic
& OtherPediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult CephalicPPPPPNote 1Note 4, 7
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac AdultPPPPPNote 1Note 4, 7
CardiacCardiac PediatricPPPPPNote 1Note 4, 7
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralPeripheral vessel
VesselOther (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler/M, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

signature

.

Concurrence of CDRH, @ffee of Davises Excalin Prescription Use (Per 21 CFR 801.109)

(Division Sign-Off) Division of Radiological Devices

510(k) Number_15093849

{8}------------------------------------------------

510(k) No.:K093849
Device Name:P2-4BA for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
AbdominalPPPPPNote 1Note 4, 7
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult CephalicPPPPPNote 1Note 4, 7
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac AdultPPPPPNote 1Note 4, 7
CardiacCardiac PediatricPPPPPNote 1Note 4, 7
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared under K092159; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: BM, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppier/M, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

signature

Concurrence of CDRH, @ffice of Bevice Evaluation Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{9}------------------------------------------------

510(k) No.:K093849
Device Name:P2-4AC for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
AbdominalPPPPPNote 1Note 4, 7
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult CephalicPPPPPNote 1Note 4, 7
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac AdultPPPPPNote 1Note 4, 7
CardiacCardiac PediatricPPPPPNote 1Note 4, 7
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler/M, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

Concurrence of CDRH, Office of Device Evaluation (OBB) Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{10}------------------------------------------------

510(k) No.:K093849
Device Name:MPT4-7 for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColor Doppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal Imaging& OtherFetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginalTrans-urethral
Trans-esoph. (non-Cardiac)PPPPNote 1Note 7, 8
Musculo-skel. (Convent.)Musculo-skel. (Superfic.)Intra-luminalOther (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)NNNNNote 1Note 7, 8
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared under K092159; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler/M, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, breast, scrotum and penis in adult, pediatic and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

DNR


Concurrence of CDRH, Office of Berice Brahaution Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{11}------------------------------------------------

510(k) No.:K093849
Device Name:LT4-7 for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
Abdominal
Intra-operative (See Note 6)NNNNNote INote 8, 9
Intra-operative (Neuro.)NNNNNote INote 8, 9
Fetal Imaging& OtherLaparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared by FDA; E= added under Appendix E
N= new indication; P= previously cleared by FDA; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 3. Includes inventory monitoring of router.
Note 4. Color M mode.

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

Concurrence of CDRH, Office of Device Evaluation (OBE) Prescription Use (Per 21 CFR 801.109)

(Division Sign-Off)
Division of Radiological Devices

510(k) Number K093849

{12}------------------------------------------------

Ko 83847 510(k) No .: Device Name:

LS5-13 for use with ACCUVIX V10

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: Clinical Application Mode of Operation (includes simultaneous B-mode) Specific B General M PWD CWD Color Combined Other (Track I only) (Tracks I & III) Doppler* (Spec.) (Spec.) Ophthalmic Ophthalmic Fetal (See Note 3) Abdominal Intra-operative (See Note 6) P P P P Note 8, 9 Note l Intra-operative (Neuro.) P P P P Note 8, 9 Note l Fetal Imaging Laparoscopic & Other Pediatric P P P p Note 8, 9 Note I Small Organ (See Note 5) P P P P Note 1 Note 8, 9 Neonatal Cephalic P P P P Note l Note 8, 9 Adult Cephalic Trans-rectal Trans-vaginal Trans-urethral Trans-esoph. (non-Cardiac) Musculo-skel. (Convent ) P P P P Note l Note 8, 9 Musculo-skel. (Superfic.) P P P P Note l Note 8, 9 Intra-luminal Other (spec.) Cardiac Adult Cardiac Cardiac Pediatric Trans-esophageal (Cardiac) Other (spec.) Peripheral Peripheral vessel P P P P Note I Note 5, 6, 9 Vessel Other (spec.)

N= new indication; P= previously cleared under K060087; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: BM, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatic and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

D.L.P.

Concurrence of CDRH, Office of Bevice Evaluatia Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{13}------------------------------------------------

Ko93849

510(k) No .: Device Name:

L8-15IS for use with ACCUVIX V10 Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
GeneralSpecificBMPWDCWDColorCombined*Other
(Track I only)(Tracks I & III)Doppler*(Spec.)(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal ImagingLaparoscopic
& OtherPediatricPPPPPNote 1Note 2, 5, 6, 9
Small Organ (See Note 5)PPPPPNote 1Note 2, 5, 6, 9
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)PPPPPNote 1Note 2, 5, 6, 9
Musculo-skel. (Superfic.)PPPPPNote 1Note 2, 5, 6, 9
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralPeripheral vesselPPPPPNote 1Note 2, 5, 6, 9
VesselOther (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode.

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatic and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

signature

Concurrence of CDRH, Gifter a Clouico Frielacati Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{14}------------------------------------------------

510(k) No.:K093849
Device Name:L7-16IS for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
PediatricPPPPNote 1Note 2, 5, 6, 9
Small Organ (See Note 5)PPPPNote 1Note 2, 5, 6, 9
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)PPPPNote 1Note 2, 5, 6, 9
Musculo-skel. (Superfic.)PPPPNote 1Note 2, 5, 6, 9
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vesselPPPPNote 1Note 2, 5, 6, 9
Other (spec.)

N= new indication; P= previously cleared under K092159; E= added under Appendix E

Additional Comments:

i

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

S.H. Ahn

Concurrence of CDRH, @ffice of Device Eurolestic Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{15}------------------------------------------------

K093849
510(k) No.:
Device Name: L6-12IS for use with ACCUVIX V10
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal Imaging& OtherFetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Laparoscopic
PediatricPPPPNote 1Note 2, 5, 6, 7, 9
Small Organ (See Note 5)PPPPNote.1Note 2, 5, 6, 7, 9
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)PPPPNote 1Note 2, 5, 6, 7, 9
Musculo-skel. (Superfic.)PPPPNote 1Note 2, 5, 6, 7, 9
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vesselPPPPNote 1Note 2, 5, 6, 7, 9
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

AdyR

Concurrence of CDRH, @ Carles Beach as Encludes How 10 DID Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{16}------------------------------------------------

510(k) No.: K093849Device Name: L5-13IS for use with ACCUVIX V10Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
General(Track I only)Clinical ApplicationSpecific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)AbdominalIntra-operative (See Note 6)Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
PediatricPPPPNote 1Note 2, 5, 6, 7, 9
Small Organ (See Note 5)Neonatal CephalicPPPPNote 1Note 2, 5, 6, 7, 9
Adult CephalicTrans-rectal
Trans-vaginalTrans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)PPPPNote 1Note 2, 5, 6, 7, 9
Musculo-skel. (Superfic.)PPPPNote 1Note 2, 5, 6, 7, 9
Intra-luminalOther (spec.)
CardiacCardiac AdultCardiac Pediatric
Trans-esophageal (Cardiac)Other (spec.)
PeripheralVesselPeripheral vesselOther (spec.)PPPPNote 1Note 2, 5, 6, 7, 9

N= new indication; P= previously cleared under K092159; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatic and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

signature

Concurrence of CDRH, Office of Barrison Eurolas 14 Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{17}------------------------------------------------

510(k) No.:K093849
Device Name:L5-12/50EP for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal Imaging& OtherFetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Laparoscopic
PediatricPPPPNote 1Note 2, 5, 6, 7, 9
Small Organ (See Note 5)PPPPNote 1Note 2, 5, 6, 7, 9
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)PPPPNote 1Note 2, 5, 6, 7, 9
Musculo-skel. (Superfic.)PPPPNote 1Note 2, 5, 6, 7, 9
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vesselPPPPNote 1Note 2, 5, 6, 7, 9
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

Signature

Concurrence of CDRH, Office of Bevice Evanianon (ODE) LODV) Prescription Use (Per 21 CFR 801.109)

(Division Sign-Off)
Division of Radiological Devices

510(k) Number K093849

{18}------------------------------------------------

510(k) No.:K093849
Device Name:L4-7EL for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
PediatricPPPPNote 1Note 2, 5, 6, 9
Small Organ (See Note 5)PPPPNote 1Note 2, 5, 6, 9
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)PPPPNote 1Note 2, 5, 6, 9
Musculo-skel. (Superfic.)PPPPNote 1Note 2, 5, 6, 9
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vesselPPPPNote 1Note 5, 6, 9
Other (spec.)

N= new indication; P= previously cleared under K092159; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler/M, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

Concurrence of CDRH, Office of Davice Evaluation ( Prescription Use (Per 21 CFR 801.109)

signature

510(k) Number K093849

{19}------------------------------------------------

K073849

510(k) No .: Device Name:

NEV4-9ES for use with ACCUVIX V10

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: Clinical Application Mode of Operation (*includes simultaneous B-mode) ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------

General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectalPPPPNote INote 2, 7, 8
Trans-vaginalPPPPNote 1Note 2, 7, 8
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: BM, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

signature

Concurrence of CDRH, Office of Device Evaluation (ODE) (ODE) Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{20}------------------------------------------------

510(k) No.:K093849
Device Name:NER4-9ES for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColor Doppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal Imaging& OtherFetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectalPPPPNote 1Note 2, 7, 8
Trans-vaginalPPPPNote 1Note 2, 7, 8
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec:)
PeripheralVesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler; B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

DSA

Concurrence of CDRH, Office of Borico Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{21}------------------------------------------------

510(k) No.:K093849
Device Name:EV4-9/10ED for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Fetal Imaging& OtherIntra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectalPPPPNote 1Note 2, 7, 8
Trans-vaginalPPPPNote 1Note 2, 7, 8
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared under K092159; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3. Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

Signature

Concurrence of CDRH, @ffice of Desice Luces of Concerted Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{22}------------------------------------------------

K093849 510(k) No .:

Device Name: Intended Use:

. જું

ER4-9/10ED for use with ACCUVIX.V10

Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: Clinical Application Mode of Operation (includes simultaneous B-mode) General Specific B PWD M CWD Color Combined Other (Track I only) (Tracks I & III) Doppler* (Spec.) (Spec.) Ophthalmic Ophthalmic Fetal (See Note 3) Abdominal Intra-operative (See Note 6) Intra-operative (Neuro.) Fetal Imaging Laparoscopic Pediatric & Other Small Organ (See Note 5) Neonatal Cephalic Adult Cephalic Trans-rectal P P P P Note I Note 2, 7, 8 Trans-vaginal P P P P Note 1 Note 2, 7, 8 Trans-urethral Trans-esoph. (non-Cardiac) Musculo-skel. (Convent.) Musculo-skel. (Superfic.) Intra-luminal Other (spec.) Cardiac Adult Cardiac Cardiac Pediatric Trans-esophageal (Cardiac) Other (spec.) Peripheral Peripheral vessel Vessel Other (spec.)

N= new indication; P= previously cleared under K092159; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

Signature

Concurrence of CDRH, Office of Barries Exclusion (0) ) Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{23}------------------------------------------------

510(k) No.:K093849
Device Name:EC4-9IS for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
Ophthalmic
Fetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Fetal Imaging& OtherIntra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectalPPPPNote 1Note 2, 7, 8
Trans-vaginalPPPPNote '1Note 2, 7, 8
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler/M, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

S.A.B

Concurrence of CDRH, SHIP Collection Concurse Concurse Prescription Use (Per 21 CFR 801,109)

510(k) Number K073849

{24}------------------------------------------------

510(k) No.:K093849
Device Name:C4-9/10ED for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)PPPPNote 1Notes 2, 7, 8
AbdominalPPPPNote.1Notes 2, 7, 8
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
PediatricPPPPNote 1Notes 2, 7, 8
Small Organ (See Note 5)PPPPNote 1Notes.2, 7, 8
Neonatal CephalicPPPPNote 1Notes 2, 7, 8
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vesselPPPPNote 1Notes 2, 7, 8
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

DSA

Concurrence of CDRH, @fferse Bouis ไ Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{25}------------------------------------------------

Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
General(Track I only)Ophthalmic
Fetal Imaging& OtherFetal (See Note 3)PPPPNote 1Notes 2, 7
AbdominalPPPPNote 1Notes 2, 7
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Laparoscopic
PediatricPPPPNote 1'Notes 2, 7
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralPeripheral vessel

N= new indication; P= previously cleared under K070813; E=added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler/M, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

ASL

i

Concurrence of CDRH; Office of Device Evaluation (@B Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{26}------------------------------------------------

510(k) No.:K093849
Device Name:C2-6IC for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)PPPPNote 1Notes 2, 7, 8
AbdominalPPPPNote 1Notes 2, 7, 8
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
PediatricPPPPNote 1Notes 2, 7, 8
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac.Cardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1 . B/M, B/PWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

D.A

Concurrence of CDRH, Office of Device Evaluation (ODE Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{27}------------------------------------------------

Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General (Track I only)Specific (Tracks I & III)BMPWDCWDColor Doppler*Combined* (Spec.)Other (Spec.)
OphthalmicOphthalmic
Fetal Imaging & OtherFetal (See Note 3)PPPPPNote 1Notes 2, 7, 8
AbdominalPPPPNote 1Notes 2, 7, 8
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Laparoscopic
PediatricPPPPNote 1Notes 2, 7, 8
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
Peripheral VesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: BM, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

D.A.B

Concurrence of CDRH, Office of Bevice Evaluatis Prescription Use (Per 21 CFR 801.109)

. 510(k) Number K093849

{28}------------------------------------------------

510(k) No.:K 093849
Device Name:V6-12 for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows
Clinical ApplicationMode of Operation (* includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
Abdominal
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
PediatricPPPPNote 1Note 2, 5, 6, 9
Small Organ (See Note 5)PPPPNote: INote 2, 5, 6, 9
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)PPPPNote 1Note 2, 5, 6, 9
Musculo-skel. (Superfic.)PPPPNote 1Note 2, 5, 6, 9
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vesselPPPPNote 1Note 5, 6, 9
Other (spec.)

Ne new indication; P= previously cleared under K092159; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler/M, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

Concurrence of CDRH, Office of Device Evaluation (ODE)(OIVD)
Prescription Use (Per 21 CFR 801.109)

(Division Sign-Off)
Division of Radiological Devices

5.10(k) Number K093849

{29}------------------------------------------------

Clinical ApplicationDiagnostic ultrasound imaging or fluid flow analysis of the human body as follows:Mode of Operation (*includes simultaneous B-mode)
GeneralTrack I only)Specific(Tracks I & II)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)Abdominal
Intra-operative (See Note 6)Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopicPediatric
Small Organ (See Note 5)Neonatal Cephalic
Adult Cephalic
Trans-rectalTrans-vaginalPPPPPPPPNote 1Note 1Notes 2, 7, 8Notes 2, 7. 8
Trans-urethralTrans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)Musculo-skel. (Superfic.)
Intra-luminalOther (spec.)
Cardiac Adult
CardiacCardiac PediatricTrans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vesselOther (spec.)

new indication; P= previously cleared under K092159; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

· Note 9: Panoramic imaging

Concurrence of CDRH, Office of Device Evaluation (ODT) (C

Prescription Use (Per 21 CFR 801.109)

510(k) Number K093849

{30}------------------------------------------------

Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)AbdominalIntra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal Imaging& OtherLaparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectalPPPPNote 1Notes 2, 7, 8
Trans-vaginalPPPPNote 1Notes 2, 7. 8
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1: B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

Concurrence of CDRH, Office of Device Evaluation (30) Prescription Use (Per 21 CFR 801.109)

Ate

510(k) Number K093849

{31}------------------------------------------------

510(k) No.:K093849
Device Name:3D4-8ET for use with ACCUVIX V10
Intended Use:Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows
Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
Ophthalmic
Fetal (See Note 3)PPPPNote 1Notes 2, 7, 8
AbdominalPPPPNote 1Notes 2, 7, 8
Fetal Imaging& OtherIntra-operative (See Note 6)
Intra-operative (Neuro.)
Laparoscopic
PediatricPPPPNote 1Notes 2, 7, 8
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note I: B/M, B/PWD, B/Color Doppler, B/PWD/Color Doppler, B/Color Doppler/M, B/Color Doppler/CWD Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatic and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

Concurrence of CDRH, Offles (OD/V
Prescription Use (Per 21 CFR 801.109)

(Division Sign-Off)
Division of Radiological Devices

510(k) Number K093849

{32}------------------------------------------------

K093849

510(k) No .: Device Name:

3D2-6ET for use with ACCUVIX V10

Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: Intended Use:

Clinical ApplicationMode of Operation (*includes simultaneous B-mode)
GeneralSpecificBMPWDCWDColorCombined*Other
(Track I only)(Tracks I & III)Doppler*(Spec.)(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)Pம்PpNote 1Notes 2, 7, 8
AbdominalPPPPNote 1Notes 2, 7, 8
Intra-operative (See Note 6)
Intra-operative (Neuro.)
Fetal ImagingLaparoscopic
&. OtherPediatricPPPPNote 1Notes 2, 7, 8
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethrai
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralPeripheral vessel
VesselOther (spec.)

N= new indication; P= previously cleared under K070813; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

Note 1 . B/M, B/PWD, B/CWD, B/Color Doppler, B/PWD/Color Doppler/M, B/Color Doppler/M, B/Color Doppler/CWD

Note 2: Includes imaging for guidance of biopsy

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

Concurrence of CDRH,
Prescription Use (Per 21 CFR 801.109)

(Division Sign-Off)
Division of Radiological Devices

510(k) Number K093849

{33}------------------------------------------------

Section 1.3 INDICATIONS FOR USE

General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDoppler*Combined*(Spec.)Other(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)PPPPPNote INotes 2, 7, 8
AbdominalPPPPPNote 1Notes 2, 7, 8
Intra-operative (See Note 6)NNNNNNote INote 7, 8, 9
Intra-operative (Neuro.)NNNNNNote 1Note 7, 8, 9
Fetal Imaging& OtherLaparoscopic
PediatricPPPPPNote 1Note 2,4,5,6,7,8,9
Small Organ (See Note 5)PPPPPNote INote 2,5,6,7,8,9
Neonatal CephalicPPPPPNote 1
Adult CephalicPPPPPNote 1Note 4, 7
Trans-rectalPPPPPNote 1Note 2, 3, 7, 8
Trans-vaginalPPPPPNote 1Note 2, 3, 7, 8
Trans-urethral
Trans-esoph. (non-Cardiac)NNNNNNote 1Notes 7, 8
Musculo-skel. (Convent.)PPPPPNote 1Note 2,5,6,7, 8,
Musculo-skel. (Superfic.)PPPPPNote 1Note 2,5,6,7, 8,
Intra-luminal
Other (spec.)
CardiacCardiac AdultPPPPPNote 1Note 4, 7
Cardiac PediatricPPPPPNote 1Note 4, 7
Trans-esophageal (Cardiac)NNNNNNote 1Notes 7, 8
Other (spec.)
PeripheralVesselPeripheral vesselPPPPPNote 1Note 5, 6, 7, 9
Other (spec.)

Note 3: Includes infertility monitoring of follicle development

Note 4: Color M-mode

Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients

Note 6: Abdominal organs and peripheral vessel

Note 7: Tissue Harmonic Imaging (THI)

Note 8: 3D imaging

Note 9: Panoramic imaging

D.S.C.

Concurrence of CDRH, @Heart Desice Emissation (OBB) Prescription Use (Per 21 CFR 801.109)

510(k) Number K09849

§ 892.1550 Ultrasonic pulsed doppler imaging system.

(a)
Identification. An ultrasonic pulsed doppler imaging system is a device that combines the features of continuous wave doppler-effect technology with pulsed-echo effect technology and is intended to determine stationary body tissue characteristics, such as depth or location of tissue interfaces or dynamic tissue characteristics such as velocity of blood or tissue motion. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.(b)
Classification. Class II.