K Number
K013723
Date Cleared
2002-02-06

(89 days)

Product Code
Regulation Number
892.1570
Reference & Predicate Devices
N/A
Predicate For
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use

Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:
General (Track I only), Specific (Tracks I & III)
Mode of Operation: B, M, Pulsed Doppler, Continuous Wave Doppler, Color Doppler, Combined (Spec.), Other (Spec.)
Other (Spec.) includes Amplitude Doppler, Harmonic Imaging and 3D Imaging.
Specific clinical applications vary by transducer.

Device Description

The Hitachi EUB-6500 Diagnostic Ultrasound Scanner is a Track 3 diagnostic ultrasound pulsed Doppler and pulsed echo imaging system capable of the following operating modes: B, M, Pulsed Doppler, Continuous Wave Doppler, Color Flow (including Amplitude Doppler). It is also intended for harmonic imaging, superficial musculoskeletal imaging, and 3D imaging.

AI/ML Overview

The provided text does not contain information about acceptance criteria or specific studies to prove device performance for the Hitachi EUB-6500 Diagnostic Ultrasound Scanner.

The document is a 510(k) premarket notification letter from the FDA, and it focuses on:

  • Device Description: A general overview of the Hitachi EUB-6500's capabilities and operating modes.
  • Safety Compliance: Statements regarding adherence to NEMA and IEC standards for acoustic output and general electrical safety.
  • Substantial Equivalence Determination: The FDA's finding that the device is substantially equivalent to legally marketed predicate devices.
  • Intended Use Tables: Detailed tables that outline the specific clinical applications and modes of operation for various transducers used with the EUB-6500. For each application, "N" indicates a new indication, and subscripts provide additional context (e.g., "Na" for abdominal imaging including biopsy guidance).
  • Post-Clearance Special Report Requirement: A condition for marketing requiring submission of acoustic output measurements from production line devices.

Therefore, I cannot fulfill your request to describe acceptance criteria and associated studies, sample sizes, data provenance, number of experts, adjudication methods, MRMC studies, standalone performance, or ground truth establishment for the Hitachi EUB-6500 based on the provided text.

This document is primarily a regulatory communication confirming marketing clearance based on substantial equivalence, not a performance study report.

{0}------------------------------------------------

FEB 0 6 2002

SUMMARY OF SAFETY AND EFFECTIVENESS Hitachi EUB-6500 Diagnostic Ultrasound Scanner

Device Description

The Hitachi EUB-6500 Diagnostic Ultrasound Scanner is a Track 3 diagnostic ultrasound pulsed Doppler and pulsed echo imaging system capable of the following operating modes: B, M, Pulsed Doppler, Continuous Wave Doppler, Color Flow (including Amplitude Doppler). It is also intended for harmonic imaging, superficial musculoskeletal imaging, and 3D imaging.

Safety

As a Track 3 ultrasound device, the Hitachi EUB-6500 Diagnostic Ultrasound Scanner complies with the "Standard for Real-Time Display of Thermal and Mechanical Acoustic Output Indices on Diagnostic Ultrasound Equipment (1992)", published by NEMA as UD-3. With respect to limits on acoustic outputs, the Hitachi EUB-6500 Diagnostic Ultrasound Scanner complies with the guideline limits set in the April 14, 1994, Revision of 510(k) Diagnostic Ultrasound Guidance.

With regard to general safety, the Hitachi EUB-6500 Diagnostic Ultrasound Scanner is designed to comply with IEC 60601-1 (1998) Medical Electrical Equipment, Part 1, General Requirements for Safety.

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

Image /page/1/Picture/1 description: The image is a black and white logo for the U.S. Department of Health & Human Services. The logo features a stylized abstract symbol resembling a bird or a person reaching out, with three curved lines forming the body and arm. The symbol is enclosed within a circular border, and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" is arranged around the upper half of the circle.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

FEB 0 6 2002

Mr. Walter Weyburne Regulatory Affairs Hitachi Medical Corporation of America 660 White Plains Road TARRYTOWN NY 10591

Re: K013723

Trade Name: EUB-6500 Diagnostic Ultrasound Scanner Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Product Code: 90 IYN Regulation Number: 21 CFR 892.1560 Regulation Name: Ultrasonic pulsed echo imaging system Product Code: 90 IYO Regulation Number: 21 CFR 892.1570 Regulation Name: Diagnostic Ultrasonic transducer Product Code: 90 ITX Regulatory Class: II Dated: January 24, 2002 Received: January 25, 2002

Dear Mr. Weyburne:

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 EUB-6500 Diagnostic Ultrasonic Scanner, as described in your premarket notification:

{2}------------------------------------------------

Transducer Model Number

EUP-B314 EUP-C514 EUP-ES322 EUP-ESS2M EUP-ES533 EUP-F531 EUP-L54M EUP-L53S EUP-OL334 EUP-R53W EUP-S50 EUP-TC3 EUP-U533 EUP-VS3W

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, you 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

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

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 nothleation. THE PDF Intention 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 If you tester of Compliance at (301) 594-4591. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). Other general information on your responsibilities under the notification (2) Stained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or at (301) 443-6597 or at its Internet address "http://www.fda.gov/cdrh/dsmamain.html".

If you have any questions regarding the content of this letter, please contact Rodrigo C. Perez at (301) 594-1212.

Sincerely yours,

David a. Leipson

for

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

Enclosure(s)

{4}------------------------------------------------

System:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other**(Spec.)
OphthalmicOphthalmic
FetalNNNNNNN
AbdominalNaNaNaNaNaNaNa
Intra-operative (Spec.)NbNbNbNbNbNbNb
Intra-operative (Neuro.)NNNNNNN
LaparoscopicNNNNNN
PediatricNNNNNNN
Small Organ (Spec.)NdNdNdNdNdNd
Neonatal CephalicNNNNNN
Fetal Imaging& OtherAdult CephalicNNNNNNN
Trans-rectalNhNhNhNhNhNh
Trans-vaginalNfNfNfNfNfNf
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)NNNNNN
Musculo-skel. (Superfic.)NNNNNN
Intra-luminal
Other (spec.)
CardiacCardiac AdultNNNNNNN
Cardiac PediatricNNNNNNN
Trans-esophageal (card.)NgNgNgNgNgNg
Other (spec.)
PeripheralVesselPeripheral vesselNNNNNNN
Other (spec.)

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

** Amplitude Doppler, Harmonic Imaging and 3D Imaging.

Additional Comments:

Subscript "a": Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures (including amniocentesis).

Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.

Subscript "b": Includes imaging for guidance of transrectal biopsy.

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE)

Vorin G. Kynn
Minister of Finance

(Division Sign Off) Division of Reproductive, Abdominal, ENT and Radiological Devices

510(k) Number: K122015

Prescription Use (Per 21 CFR 801.109)

Section 4.3 Page 1 / 15

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System: Transducer:

EUB-6500 EUP-B314

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined *(Spec.)Other **(Spec.)
OphthalmicOphthalmic
FetalNNNNNN
AbdominalNaNaNaNaNaNa
Intra-operative (Spec.)NbNbNbNbNbNb
Intra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (Spec.)
Neonatal Cephalic
Fetal Imaging& OtherAdult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (card.)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

** Amplitude Doppler and 3D Imaging.

Additional Comments:

Subscript "a": Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures (including amniocentesis).

Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.

script. D. Includes masking for guidance of anatomical display.
PLEASE DO NOT WRITE BELOW THIS LINE. FOR MITTEE ON ALL NOTES.

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

David A. Heyman
Division Sign (4a)

(Division Sign-Off) Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number:_

Prescription Use (Per 21 CFR 801.109)

Section 4.3 Page 2 / 15

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

System: Transducer:

EUP-C514

EUB-6500

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other**(Spec.)
OphthalmicOphthalmicN
FetalNNNNNN
AbdominalNaNaNaNaNaNa
Intra-operative (Spec.)
Intra-operative (Neuro.)
Laparoscopic
PediatricNNNNNN
Small Organ (Spec.)NdNdNdNdNdNd
Neonatal Cephalic
Fetal Imaging& OtherAdult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (card.)
Other (spec.)
PeripheralPeripheral vessel
VesselOther (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

** Amplitude Doppler, Harmonic Imaging and 3D Imaging.

Additional Comments:

Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.

( LEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED! Concurrence of CDRH, Office of Device Evaluation (ODE)

David A. Seymour

(Division Sign Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number:

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

System: Transducer:

EUB-6500 EUP-ES322

College of the product and the production of the

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other**(Spec.)
OphthalmicOphthalmic
Fetal
Abdominal
Intra-operative (Spec.)
Intra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (Spec.)
Neonatal Cephalic
Fetal Imaging& OtherAdult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (card.)NNNNNNN
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

**Amplitude Doppler and 3D Imaging.

Additional Comments:

Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures
(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery
(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

Emin A. Seymore
(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number:

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

System: Transducer: EUB-6500

EUP-ES52M

Intended use: Diagnostic ultrasound imaging or fluid flow analysis it the human body as follows:

Mode of Operation Clinical Application Other ** Combined* Color CAMD PWD B M Specific General (Spec.) (Spec.) Doppler (Tracks I & III) (Track I only) Ophthalmic Ophthalmic Fetal Abdominal Intra-operative (Spec.) Intra-operative (Neuro.) Laparoscopic Pediatric Small Organ (Spec.) Neonatal Cephalic Adult Cephalic Fetal Imaging Trans-rectal & Other Trans-vaginal Trans-urethral Trans-esoph. (non-Card.) Musculo-skel. (Convent.) Musculo-skel. (Superfic.) Intra-luminal Other (spec.) Cardiac Adult Cardiac Pediatric Cardiac N N N N N N N Trans-esophageal (card.) Other (spec.) Peripheral vessel Peripheral Other (spec.) Vessel

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

** Amplitude Doppler and 3D Imaging.

Additional Comments:

Additional Comments:
Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures
(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery
(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF N Concurrence of CDRH, Office of Device Evaluation (ODE)

Cl. J. de Jong

David G. Wegner
(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number:

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

System: Transducer:

EUB-6500 EUP-ES533

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other **(Spec.)
OphthalmicOphthalmic
Fetal
Abdominal
Intra-operative (Spec.)
Intra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (Spec.)
Neonatal Cephalic
Fetal Imaging& OtherAdult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (card.)NgNgNgNgNgNgNg
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

** Amplitude Doppler and 3D Imaging.

Additional Comments:

Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

David A. Segerson
(Division Sign-off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number:

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

System: Transducer: EUB-6500

EUP-F531

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other**(Spec.)
OphthalmicOphthalmic
FetalNNNNNNN
AbdominalNbNbNbNbNbNbNb
Intra-operative (Spec.)NNNNNNN
Intra-operative (Neuro.)NNNNNNN
Laparoscopic
PediatricNNNNNNN
Small Organ (Spec.)NcNcNcNcNcNcNc
Neonatal CephalicNNNNNNN
Fetal Imaging& OtherAdult Cephalic
Trans-rectalNNNNNNN
Trans-vaginalNNNNNNN
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (card.)
Other (spec.)
PeripheralVesselPeripheral vesselNNNNNNN
Other (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

** Amplitude Doppler and 3D Imaging.

Additional Comments:

Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.

Subscr

(PLEASE DO NOT WRITE BELOW THIS MINE CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE)

Emil A. Hegner
(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number:

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

System: Transducer: EUB-6500

EUP-L54M

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other**(Spec.)
OphthalmicOphthalmic
Fetal
AbdominalNaNaNaNaNaNa
Intra-operative (Spec.)
Intra-operative (Neuro.)NNNNNN
Laparoscopic
PediatricNNNNNN
Small Organ (Spec.)NdNdNdNdNdNd
Neonatal Cephalic
Fetal Imaging& OtherAdult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)NNNNNN
Musculo-skel. (Superfic.)NNNNNN
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (card.)
Other (spec.)
PeripheralVesselPeripheral vesselNNNNNN
Other (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

** Amplitude Doppler and 3D Imaging.

Additional Comments:

Subscript "a": Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures
(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery
(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.

Includes imaging for guidance of transrectal biopsy. Subscript "h": (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

David A. Symon

(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number:

Prescription Use (Pcr 21 CFR 801.109)

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

System: Transducer: EUB-6500

EUP-L53S

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other**(Spec.)
OphthalmicOphthalmic
Fetal
AbdominalNaNaNaNaNaNa
Intra-operative (Spec.)
Intra-operative (Neuro.)NNNNNN
Laparoscopic
PediatricNNNNNN
Small Organ (Spec.)NdNdNdNdNdNd
Neonatal Cephalic
Fetal Imaging& OtherAdult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)NNNNNN
Musculo-skel. (Superfic.)NNNNNN
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (card.)
Other (spec.)
PeripheralVesselPeripheral vesselNNNNNN
Other (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

** Amplitude Doppler and 3D Imaging.

Additional Comments:

Additional Comments.
Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.

Subscript "h": Includes imaging for guidance of transrectal biopsy.

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE)

David G. Hyman


(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number:

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

System: Transducer:

EUB-6500 EUP-OL334

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Mode of Operation Clinical Application PWD CNTD Color Combined* Other* M General Specific B (Spec.) Doppler (Spec.) (Track I only) (Tracks I & III) Ophthalmic Ophthalmic Fetal Abdominal Intra-operative (Spec.) Intra-operative (Neuro.) N N N N Laparoscopic N N Pediatric Small Organ (Spec.) Neonatal Cephalic Fetal Imaging Adult Cephalic & Other Trans-rectal Trans-vaginal Trans-urethral Trans-esoph. (non-Card.) Musculo-skel. (Convent.) Musculo-skel. (Superfic.) Intra-luminal Other (spec.) Cardiac Adult Cardiac Pediatric Cardiac Trans-esophageal (card.) Other (spec.) Peripheral vessel Peripheral Other (spec.) Vessel

N = new indication.

  • Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

** Amplitude Doppler and 3D Imaging.

Additional Comments:

Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.

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Subscript "e": Includes imaging for guidance of transrectal biopsy. Subscript "f": Includes imaging for guidance of transvaginal biopsy. Subscript "g": For pediatric patients.

Includes imaging for guidance of transrectal biopsy Subscript "h":

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

David A. Seymann

(Division Sign-Qff) Division of Reproductive, Abdominal, ENT and Radiological Devices

510(k) Number: K161613

Prescription Use (Per 21 CFR 801.109)

Section 4.3 Page 10 / 15

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

System: Transducer: EUB-6500

EUP-R53W

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other**(Spec.)
OphthalmicOphthalmic
Fetal Imaging& OtherFetal
Abdominal
Intra-operative (Spec.)
Intra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (Spec.)
Neonatal Cephalic
Adult Cephalic
Trans-rectalNNNNNN
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac Adult
Cardiac Pediatric
Trans-esophageal (card.)
PeripheralVesselPeripheral vessel
Other (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

**Amplitude Doppler and 3D Imaging.

Additional Comments:

Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

David Li. Mason
(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number: K033023

/

Prescription Use (Per 21 CFR 801.109)

Section 4.3 Page 11 / 15

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

System: Transducer:

EUB-6500 EUP-850

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other **(Spec.)
OphthalmicOphthalmic
FetalNNNNNNN
AbdominalNNNNNNN
Intra-operative (Spec.)
Intra-operative (Neuro.)
Laparoscopic
PediatricNNNNNNN
Small Organ (Spec.)
Neonatal Cephalic
Fetal Imaging& OtherAdult CephalicNNNNNNN
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac AdultNNNNNNN
CardiacCardiac PediatricNNNNNNN
Trans-esophageal (card.)
Other (spec.)
PeripheralVesselPeripheral vesselNNNNNNN
Other (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

** Amplitude Doppler, Harmonic Imaging and 3D Imaging.

Additional Comments:

Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDEDY
COLORIES Concurrence of CDRH, Office of Device Evaluation (ODE)

Concurrence of CDRH, Office of Device Evaluation (ODE)

David A. Larson
(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number: K013533

Prescription Use (Per 21 CFR 801.109)

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

System: Transducer:

EUB-6500 EUP-TC3

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other**(Spec.)
OphthalmicOphthalmic
Fetal
Abdominal
Intra-operative (Spec.)
Intra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (Spec.)
Neonatal Cephalic
Fetal Imaging& OtherAdult Cephalic
Trans-rectal
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
CardiacCardiac AdultN
Cardiac PediatricN
Trans-esophageal (card.)
Other (spec.)
PeripheralVesselPeripheral vesselN
Other (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

**Amplitude Doppler.

Additional Comments:

Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

David G. Symons
(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number: K161293

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

System: Transducer: EUB-6500

EUP-U533

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other **(Spec.)
OphthalmicOphthalmic
Fetal
Abdominal
Intra-operative (Spec.)
Intra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (Spec.)
Neonatal Cephalic
Fetal Imaging& OtherAdult Cephalic
Trans-rectalNhNhNhNhNhNh
Trans-vaginal
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (card.)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

**Amplitude Doppler and 3D Imaging.

Additional Comments:

Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.
(PLEASE DO NOT WRITE BELOW THIS LINE CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

David H. Leggrm


(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number: K111613

Prescription Use (Per 21 CFR 801.109)

Section 4.3 Page 14 / 15

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

System: Transducer:

EUB-6500 EUP-V53W

Intended use: Diagnostic ultrasound imaging or fluid flow analysis if the human body as follows:

Clinical ApplicationMode of Operation
General(Track I only)Specific(Tracks I & III)BMPWDCWDColorDopplerCombined*(Spec.)Other**(Spec.)
OphthalmicOphthalmic
FetalNNNNNN
Abdominal
Intra-operative (Spec.)
Intra-operative (Neuro.)
Laparoscopic
Pediatric
Small Organ (Spec.)
Neonatal Cephalic
Fetal Imaging& OtherAdult Cephalic
Trans-rectalNeNeNeNeNeNe
Trans-vaginalNfNfNfNfNfNf
Trans-urethral
Trans-esoph. (non-Card.)
Musculo-skel. (Convent.)
Musculo-skel. (Superfic.)
Intra-luminal
Other (spec.)
Cardiac Adult
CardiacCardiac Pediatric
Trans-esophageal (card.)
Other (spec.)
PeripheralVesselPeripheral vessel
Other (spec.)

N = new indication.

*Combination of each operating mode, B, M, PWD, CWD and Color Doppler.

** Amplitude Doppler and 3D Imaging.

Additional Comments:

Subscript "a":Includes imaging for guidance of percutaneous biopsy of abdominal organs and structures(including amniocentesis).
Subscript "b":Includes imaging of organs and structures exposed during surgery(excluding neurosurgery and laparoscopic procedures).
Subscript "c":Includes thyroid, parathyroid, breast, scrotum, penis.
Subscript "d":Includes thyroid, parathyroid, breast, scrotum, penis and imaging for guidance of biopsy.
Subscript "e":Includes imaging for guidance of transrectal biopsy.
Subscript "f":Includes imaging for guidance of transvaginal biopsy.
Subscript "g":For pediatric patients.
Subscript "h":Includes imaging for guidance of transrectal biopsy.

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

David A. Demme
(Division Sign-Off)

Division of Reproductive, Abdominal, ENT, and Radiological Devices

510(k) Number: K131633

Prescription Use (Per 21 CFR 801.109)

Section 4.3 Page 15 / 15

§ 892.1570 Diagnostic ultrasonic transducer.

(a)
Identification. A diagnostic ultrasonic transducer is a device made of a piezoelectric material that converts electrical signals into acoustic signals and acoustic signals into electrical signals and intended for use in diagnostic ultrasonic medical devices. Accessories of this generic type of device may include transmission media for acoustically coupling the transducer to the body surface, such as acoustic gel, paste, or a flexible fluid container.(b)
Classification. Class II.