K Number
K061213
Device Name
SONOACE PICO DIAGNOSTIC ULTRASOUND SYSTEM
Manufacturer
Date Cleared
2006-05-16

(14 days)

Product Code
Regulation Number
892.1550
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: General, OB, Gynecology, Abdomen, Fetal Heart, Renal, Neonatal, Pediatric, Vascular, Cardiac, Urology, Breast, Small Parts, Musculoskeletal applications. The system also provides for the measurement of anatomical structures and for analysis packages that provide information that is used for clinical diagnosis purposes.
Device Description
The SONOACE PICO is a general purpose, mobile, software controlled, diagnostic ultrasound system with on-screen display for themal and mechanical indices related to potential bioeffect mechanisms. Its function is to acquire ultrasound data and to display the data as B-mode, M-mode, Color Doppler, Pulsed (PW) Doppler, Power Doppler, Harmonic imaging and 3D imaging , or as a combination of these modes on the LCD monitor.
More Information

No
The document does not mention AI, ML, or related terms, and the device description focuses on standard ultrasound imaging modes.

No
The device is described as a "diagnostic ultrasound imaging or fluid flow analysis" system, and its function is to "acquire ultrasound data and to display the data" for "clinical diagnosis purposes". It does not mention any therapeutic capabilities.

Yes
The "Intended Use / Indications for Use" section explicitly states "Diagnostic ultrasound imaging" and "analysis packages that provide information that is used for clinical diagnosis purposes." The "Device Description" also labels it as a "diagnostic ultrasound system."

No

The device description explicitly states it is a "diagnostic ultrasound system," which inherently includes hardware components for generating and receiving ultrasound waves, in addition to the software control.

Based on the provided information, this device is not an IVD (In Vitro Diagnostic).

Here's why:

  • IVD Definition: In vitro diagnostics are tests performed on samples taken from the human body, such as blood, urine, or tissue, to detect diseases, conditions, or infections. They are used outside of the body.
  • Device Function: The description clearly states that the SONOACE PICO is a diagnostic ultrasound system that acquires and displays ultrasound data of the human body. This is an in vivo (within the living body) imaging technique.
  • Intended Use: The intended use describes imaging and analysis of the human body directly, not analysis of samples taken from the body.

Therefore, the SONOACE PICO falls under the category of medical imaging devices, not in vitro diagnostics.

N/A

Intended Use / Indications for Use

The SONOACE PICO system is intended for the following applications: General, OB, Gynecology, Abdomen, Fetal Heart, Renal, Neonatal, Pediatric, Vascular, Cardiac, Urology, Breast, Small Parts, Musculoskeletal applications. The system also provides for the measurement of anatomical structures and for analysis packages that provide information that is used for clinical diagnosis purposes.
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: General, Ophthalmic, Fetal, Abdominal, Intra-operative (Abdominal, vascular; Neuro.), Laparoscopic, Pediatric, Small Organ, Neonatal Cephalic, Adult Cephalic, Trans-rectal, Trans-vaginal, Trans-urethral, Trans-esoph. (non-Cardiac), Musculo-skel. (Convent.), Musculo-skel. (Superfic.), Intra-luminal, Cardiac (Adult, Pediatric, Trans-esophageal (Cardiac)), Peripheral vessel.

Product codes

90-IYN, 90-IYO, 90-ITX

Device Description

The SONOACE PICO is a general purpose, mobile, software controlled, diagnostic ultrasound system with on-screen display for themal and mechanical indices related to potential bioeffect mechanisms. Its function is to acquire ultrasound data and to display the data as B-mode, M-mode, Color Doppler, Pulsed (PW) Doppler, Power Doppler, Harmonic imaging and 3D imaging, or as a combination of these modes on the LCD monitor.

Mentions image processing

Its function is to acquire ultrasound data and to display the data as B-mode, M-mode, Color Doppler, Pulsed (PW) Doppler, Power Doppler, Harmonic imaging and 3D imaging, or as a combination of these modes on the LCD monitor.
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.

Mentions AI, DNN, or ML

Not Found

Input Imaging Modality

Ultrasound

Anatomical Site

General, OB, Gynecology, Abdomen, Fetal Heart, Renal, Neonatal, Pediatric, Vascular, Cardiac, Urology, Breast, Small Parts, Musculoskeletal, Ophthalmic, Intra-operative (Abdominal, vascular; Neuro.), Laparoscopic, Neonatal Cephalic, Adult Cephalic, Trans-rectal, Trans-vaginal, Trans-urethral, Trans-esoph. (non-Cardiac), Intra-luminal, Peripheral vessel.

Indicated Patient Age Range

Adult, pediatric and neonatal patients.

Intended User / Care Setting

Not Found

Description of the training set, sample size, data source, and annotation protocol

Not Found

Description of the test set, sample size, data source, and annotation protocol

Not Found

Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)

Not Found

Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)

Not Found

Predicate Device(s)

K013627, K043455

Reference Device(s)

Not Found

Predetermined Change Control Plan (PCCP) - All Relevant Information

Not Found

§ 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.

0

SONOACE PICO Diagnostic

MAY 16 2006

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: April 10, 2006

2. Name of the device:

Common/Usual Name:

Diagnostic Ultrasound System and Accessories

Proprietary Name:

SONOACE PICO Diagnostic Ultrasound System

Classification Names:FR NumberProduct Code
Ultrasonic Pulsed Doppler Imaging System892.155090-IYN
Ultrasound Pulsed Echo Imaging System892.156090-IYO
Diagnostic Ultrasound Transducer892.157090-ITX

3. Identification of the predicate or legally marketed device:

K013627, 11/16/2001, SA8000 Ultrasound system K043455, 12/21/2004, SA8000 SE Ultrasound system

. .. ..

4. Device Description:

The SONOACE PICO is a general purpose, mobile, software controlled, diagnostic ultrasound system with on-screen display for themal and mechanical indices related to potential bioeffect mechanisms. Its function is to acquire ultrasound data and to display the data as B-mode, M-mode, Color Doppler, Pulsed (PW) Doppler, Power Doppler, Harmonic imaging and 3D imaging , or as a combination of these modes on the LCD monitor.

510(k) Summary of Safety and Effectiveness

ATTACHMENT 1(b)

1

The SONOACE PICO 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 y -
  • -NEMA UD 2-2004 Acoustic Output Measurement Standard for Diagnostic Ultrasound Equipment
  • -NEMA UD 3-2004 Standard for Real Time Display of Thermal and Mechanical Acoustic Output Indices on Diagnostic Ultrasound Equipment
  • IEC 61157, Declaration of the acoustic output .
  • -ISO10993, Biocompatibility

5. Intended Uses:

The SONOACE PICO system is intended for the following applications: General, OB, Gynecology, Abdomen, Fetal Heart, Renal, Neonatal, Pediatric, Vascular, Cardiac, Urology, Breast, Small Parts, Musculoskeletal applications.

The system also provides for the measurement of anatomical structures and for analysis packages that provide information that is used for clinical diagnosis purposes.

6. Technological Characteristics:

The SONOACE PICO is substantially equivalent to the SA8000 Diagnostic Ultrasound System, cleared via K013627, and the SA8000 SE Diagnostic Ultrasound System, cleared via K043455. 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

510(k) Summary of Safety and Effectiveness

.. .. . . . . .

ATTACHMENT 1(b)

2

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 stylized caduceus symbol, which is a staff with two snakes coiled around it, and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged in a circular fashion around the symbol. The text is in all caps and is evenly spaced around the circle.

Public Health Service

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

MAY 1 6 2006

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

Re: K061213

Trade Name: SONOACE PICO Ultrasound System Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Regulation Number: 21 CFR 892.1560 Regulation Name: Ultrasonic pulsed echo imaging system Regulation Number: 21 CFR 892.1570 Regulation Name: Diagnostic ultrasonic transducer Regulatory Class: II Product Code: IYN, IYO, and ITX Dated: April 27, 2006 Received: May 2, 2006

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 SONOACE PICO Ultrasound System, as described in your premarket notification:

Image /page/2/Picture/11 description: The image shows a circular logo with the letters "FDA" in large, bold font in the center. Above the letters, the years "1906 - 2006" are displayed, indicating a centennial celebration. Below the letters, the word "Centennial" is written in a cursive font, and three stars are aligned beneath it. The text "FDA 100 YEARS OF CONSUMER PROTECTION" is arranged around the circular border of the logo.

3

Transducer Model Number

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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 (QS) 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 determination of substantial equivalence is granted on the condition that prior to shipping the first device. vou submit a postclearance special report. This report should contain complete information, including acoustic output measurements based on production line devices, requested in Appendix G. (enclosed) of the Center's September 30, 1997 "Information for Manufacturers Seeking Marketing Clearance of Diagnostic Ultrasound Systems and Transducers." If the special report is incomplete or contains unacceptable values (e.g., acoustic output greater than approved levels), then the 510(k) clearance may not apply to the production units which as a result may be considered adulterated or misbranded.

The special report should reference the manufacturer's 510(k) number. It should be clearly and prominently marked "ADD-TO-FILE" and should be submitted in duplicate to:

Food and Drug Administration Center for Devices and Radiological Health Document Mail Center (HFZ-401) 9200 Corporate Boulevard Rockville, Maryland 20850

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.

4

Page 2 - Mr. Job

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Mace Eacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html

If you have any questions regarding the content of this letter; please contact Andrew Kang, M.D. at (301) 594-1212.

Sincerely yours,

Nancy C brogdon

Nancy C. Brogdon Director, Division of Reproductive, Abdominal and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosures

5

Section 4.3 INDICATIONS FOR USE

DIAGNOSTIC ULTRASOUND INDICATIONS STATEMENT

061213 510(k) No .:

Device name: SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Clinical Application Mode of Operation General Specific B M PWD CWD Color Combined* Other (Track I only) (Tracks I & III) Doppler* (Spec.) (Spec.) Ophthalmic Ophthalmic Fetal (Soo Note 3) P P P P Note 1 Nate 7 6 7 8 Abdominal P P P P Note 1 Note 2, 6, 7, 8 Intra-operative (See Note 6) Intra-operative (Neuro.) Fetal Imaging Laparoscopic & Other Pediatric P P P P Note l Note 2, 5, 7, 8 P P P Small Organ (See Note 5) P Note 1 Note 2, 5, 8 N N Neonatal Cephalic N N Note l Note 2, 5, 8 Adult Cephalic P P Trans-rectal P P Note 2, 8 Note 1 Trans-vagina! P P P b Note 2, 3, 8 Note l Trans-urethral Trans-esoph. (non-Cardiac) P P Musculo-skel. (Convent.) P P Notel Note 2, 5, 8 Musculo-skel. (Superfic.) P P P P Note I Note 2, 5, 8 Intra-luminal Other (spec.) P Cardian Adult P P P Notel Note 4 Cardiac Cardiac Pediatric Trans-esophageal (Cardiac) Other (spec.) Perinheral veccal Perinheral P P P P Notel Note 7 5 8 Vessel Other (spec.)

N= new indication; P= previously cleared by FDA in K031552; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

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

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

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

Nancy Brogdon

(Division Sign-Off) D
Division of Reproductive, Abdominal,
and Radiological Devices
510(k) Number K061213

Section 4.3, Page 1 of 12

6

Kob 1213 510(k) No.: C2-4ES with SONOACE PICO Ultrasound System Device name: Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Clinical ApplicationMode of Operation
General
(Track I only)Specific
(Tracks I & III)BMPWDCWDColor
Doppler*Combined*
(Spec.)Other
(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)NNNNNote 1Note 2, 7, 8
AbdominalNNNNNote 1Note 2, 7, 8
Intra-operative
(Abdominal,
vascular)
Intra-operative (Neuro.)
Fetal Imaging
& OtherLaparoscopic
PediatricNNNNNote 1Note 2, 5, 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 AdultPPPPNote 1Note 4
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
Peripheral
VesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared by FDA in K031552; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

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

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

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

Nancy broadon

Basic Information

Section 4.3, Page 2 of 12

7

510(k) No.:

K061213

DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE STATEMENT

Device name: C2-5ET with SONOACE PICO Ultrasound System
Clinical ApplicationIntended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Mode of Operation
General
(Track I only)Specific
(Tracks I & III)BMPWDCWDColor
Doppler*Combined*
(Spec.)Other
(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)PPPPPNote 1Note 2, 7, 8
AbdominalPPPPPNote 1Note 2, 7, 8
Intra-operative
(Abdominal,
vascular)
Intra-operative (Neuro.)
Fetal ImagingLaparoscopic
& OtherPediatricPPPPPNote 1Note 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 Adult
CardiacCardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
PeripheralPeripheral vessel
VesselOther (spec.)

N= new indication; P= previously cleared by FDA in K043455; E= added under Appendix E Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

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

  • 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

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

Nancy Brigdon

一、大量的一系的意味

Division of Reproductive, Abdominal,
and Radiological Devices
510(k) Number K061213

Section 4.3, Page 3 of 12

8

510(k) No .: Device name: th SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Clinical ApplicationMode of Operation
General
(Track I only)Specific
(Tracks I & III)BMPWDCWDColor
Doppler*Combined*
(Spec.)Other
(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)PPPPNote 1Note 2, 7, 8
AbdominalPPPPNote 1Note 2, 7, 8
Intra-operative (Abdominal, vascular)
Intra-operative (Neuro.)
Fetal Imaging
& OtherLaparoscopic
PediatricPPPPNote 1Note 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 Adult
CardiacCardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
Perinheral
VesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared by FDA in K013627, K031552, K043455; E= added under Appendix E Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

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

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

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

Nancy C. Brogdon

510kl

Section 4.3, Page 4 of 12

9

KO61213 510(k) No .:

Device name: C4-7ED with SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Clinical ApplicationMode of Operation
General
(Track I only)Specific
(Tracks I & III)BMPWDCWDColor
Doppler*Combined*
(Spec.)Other
(Spec.)
OphthalmicOphthalmic
Fetal (See Note 2)PPPPNote 1Note 2, 7, 8
AbdominalPPPPNote 1Note 2, 7, 8
Intra-operative
(Abdominal,
vascular)
Intra-operative (Neuro.)
Fetal Imaging
& OtherLaparoscopic
PediatricPPPPNote 1Note 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 Adult
CardiacCardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
Perinheral
VesselPerinheral vessel
Other (spec.)

N= new indication; P= previously cleared by FDA in K990970, K012887; E= added under Appendix E Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

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

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

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

Nancy C. Brogdon

Division of Reproductive, Abdominal,
and Radiological Devices
510(k) Number K061213

Section 4.3, Page 5 of 12

10

510(k) No .:K061213A
Device name:C4-9ED with SONOACE PICO Ultrasound System
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation
GeneralSpecificBMPWDCWDColorCombined*Other
(Track I only)(Tracks I & III)Doppler*(Spec.)(Spec.)
OphthalmicOphthalmic
Fetal (See Note 2)PPPPNote 1Note 2 6 7 8
AbdominalNNNNNote 1Note 2, 6, 7, 8
Intra-operative
(Abdominal,
vascular)
Intra-operative (Neuro.)
Fetal ImagingLaparoscopic
& OtherPediatricNNNNNote 1Note 2, 5, 8
Small Organ (See Note 5)PPPPNote 1Note 2, 5, 8
Neonatal CephalicPPPPNote 1Note 2, 5, 8
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.)
PeripheralPeripheral vesselPPPPNote 1Note 2 5 8
VesselOther (spec.)

N= new indication; P= previously cleared by FDA in K043455; E= added under Appendix E Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

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

  • 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

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

Nancy C. Brogdon

(Division Sign Division of Reproductive, Abdo and Radiological Devices 510(k) Number

Section 4.3, Page 6 of 12

.

11

KO61213 510(k) No .:

Device name: EC4-9ED with SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Clinical Application Mode of Operation CWD General Specific B M PWD Color Combined* Other (Track I only) (Tracks I & III) Doppler* (Spec.) (Spec.) Ophthalmic Ophthalmic Fetal (Soo Note 3) Abdominal Intra-operative (Abdominal, vascular) Intra-operative (Neuro.) Laparoscopic Fetal Imaging Pediatric & Other Small Organ (See Note 5) Neonatal Cephalic Adult Cephalic Trans-rectal P P P P Note 1 Note 2, 8 P Trans-vaginal P P P Note I Note 2, 3, 8 Trans-urethral Trans-esoph. (non-Cardiac) Musculo-skel. (Convent.) Musculo-skel. (Superfic.) Intra-luminal Other (spec.) Cardian Adult Cardiac Cardiac Pediatric Trans-esophageal (Cardiac) Other (spec.) Perinheral Perinheral vescel Vessel Other (spec.)

N= new indication; P= previously cleared by FDA in K031552, K043455; E=added under Appendix E Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

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

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

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

Nancy Brogdon

Basic Information

(Division Sic Division of Reproductiv and Radiological Devices 510(k) Number

Section 4.3, Page 7 of 12

12

KO61218 510(k) No.:

Device name: EC4-9ES with SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Clinical ApplicationMode of Operation
General
(Track I only)Specific
(Tracks I & III)BMPWDCWDColor
Doppler*Combined*
(Spec.)Other
(Spec.)
OphthalmicOphthalmic
Fetal Imaging
& OtherFetal (See Note 3)
Abdominal
Intra-operative
(Abdominal,
vascular)
Intra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (See Note 5)
Neonatal Cephalic
Adult Cephalic
Trans-rectalPPPPNote 1Note 2, 8
Trans-vaginalPPPPNote 1Note 2, 3, 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.)
Peripheral
VesselPeripheral vessel
Other (spec.)

N=new indication; P= previously cleared by FDA in K031552, K013627; E=added under Appendix E Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

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

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

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

Nancy C. Brogdon

and Rad 510(k) Numb

Section 4.3, Page 8 of 12

13

510(k) No.:K061213
Device name: HC2-5ED with SONOACE PICO Ultrasound System
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation
General
(Track I only)Specific
(Tracks I & III)BMPWDCWDColor
Doppler*Combined*
(Spec.)Other
(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)PPPPNote1Note 2 8
AbdominalPPPPNote1Note 2, 8
Intra-operative (Abdominal,
vascular)
Intra-operative (Neuro.)
Fetal Imaging
& OtherLaparoscopic
PediatricPPPPNote1Note 2, 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 Adult
CardiacCardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
Perinheral
VesselPeripheral vessel
Other (spec.)

N= new indication; P= previously cleared by FDA in K031552; E= added under Appendix E Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

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

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

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

Nancy Broadon

Basic Information

(Division Sio Division of Reproductive and Radiological Devices 510(k) Number

Section 4.3, Page 9 of 12

14

510(k) No.:

DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE STATEMENT

KO61213

Device name: HL5-9ED with SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

| | Clinical Application
Mode of Operation | | | | | | | |
|---------------------------|---------------------------------------------|---|---|-----|-----|-------------------|----------------------|------------------|
| General
(Track I only) | Specific
(Tracks I & III) | B | M | PWD | CWD | Color
Doppler* | Combined*
(Spec.) | Other
(Spec.) |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetal ( See Note 3 ) | | | | | | | |
| | Abdominal | | | | | | | |
| | Intra-operative
(Abdominal,
vascular) | | | | | | | |
| | Intra-operative (Neuro.) | | | | | | | |
| Fetal Imaging
& Other | Laparoscopic | | | | | | | |
| | Pediatric | P | P | P | | P | Note 1 | Note 2, 5, 8 |
| | Small Organ ( See Note 5 ) | P | P | P | | P | Note 1 | Note 2, 5, 8 |
| | Neonatal Cephalic | | | | | | | |
| | Adult Cephalic | | | | | | | |
| | Trans-rectal | | | | | | | |
| | Trans-vaginal | | | | | | | |
| | Trans-urethral | | | | | | | |
| | Trans-esoph. (non-Cardiac) | | | | | | | |
| | Musculo-skel. (Convent.) | P | P | P | | P | Note 1 | Note 2, 5, 8 |
| | Musculo-skel. (Superfic.) | P | P | P | | P | Note 1 | Note 2, 5, 8 |
| | Intra-luminal | | | | | | | |
| | Other (spec.) | | | | | | | |
| | Cardiac Adult | | | | | | | |
| Cardiac | Cardiac Pediatric | | | | | | | |
| | Trans-esophageal (Cardiac) | | | | | | | |
| | Other (spec.) | | | | | | | |
| Perinheral
Vessel | Perinheral vessel | P | P | P | | P | Note 1 | Note 2, 5, 8 |
| | Other (spec.) | | | | | | | |

N= new indication; P= previously cleared by FDA in K013627, K031552, K043455; E= added under Appendix E Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

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

  • 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

Basic Information

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

Nancy Brogdon

(Division Sign-Division of Reproductive, Abde and Radiological Devices 510(k) Number

Section 4.3, Page 10 of 12

15

510(k) No.:K061213
Device name:L5-9EC with SONOACE PICO Ultrasound System
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation
General
(Track I only)Specific
(Tracks I & III)BMPWDCWDColor
Doppler*Combined*
(Spec.)Other
(Spec.)
OphthalmicOphthalmic
Fetal Imaging
& OtherFetal (See Note 3)
Abdominal
Intra-operative (Abdominal,
vascular)
Intra-operative (Neuro.)
Laparoscopic
PediatricPPPPNote 1Note 2, 5, 8
Small Organ (See Note 5)PPPPNote 1Note 2, 5, 8
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)PPPPNote 1Note 2, 5, 8
Musculo-skel. (Superfic.)PPPPNote 1Note 2, 5, 8
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
Peripheral
VesselPeripheral vesselPPPPNote 1Note 2 & 8
Other (spec.)
VesselOther (spec.)
-----------------------

N= new indication; P= previously cleared by FDA in K013627; E= added under Appendix E

Additional Comments:

Color Doppier includes Power (Amplitude) Doppler

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

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

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

Nancy C Broadon

(Division Sign-Off) Division of Reproductive, Abdom and Radiological Devices 510(k) Number

Section 4.3, Page 11 of 12

16

| K061213

510(k) No.:
Device name: L5-9EE with SONOACE PICO Ultrasound System
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical ApplicationMode of Operation
General
(Track I only)Specific
(Tracks I & III)BMPWDCWDColor
Doppler*Combined*
(Spec.)Other
(Spec.)
OphthalmicOphthalmic
Fetal (See Note 3)
Abdominal
Intra-operative
(Abdominal,
vascular)
Intra-operative (Neuro.)
Fetal Imaging
& OtherLaparoscopic
PediatricPPPPNote 1Note 2, 5, 8
Small Organ (See Note 5)PPPPNote 1Note 2, 5, 8
Neonatal Cephalic
Adult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Cardiac)
Musculo-skel. (Convent.)PPPPNote 1Note 2, 5, 8
Musculo-skel. (Superfic.)PPPPNote 1Note 2, 5, 8
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (Cardiac)
Other (spec.)
Peripheral
VesselPeripheral vesselPPPPNote 1Note 2, 8
Other (spec.)

N= new indication; P= previously cleared by FDA in K043455; E= added under Appendix E

Additional Comments:

Color Doppler includes Power (Amplitude) Doppler

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

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

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

Nancy Chogdon

Basic Information

(Division Sign Division of Reproductive, A and Radiological Devices " : " : " : imhor

Section 4.3, Page 12 of 12