Medical Device Manufacturer · US , Cherry Hill , NJ

F.M. Wiest USA, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1986

Total

Cleared

Denied

F.M. Wiest USA, Inc. has 12 FDA 510(k) cleared medical devices. Based in Cherry Hill, US.

Historical record: 12 cleared submissions from 1986 to 1994. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by F.M. Wiest USA, Inc. Filter by specialty or product code using the sidebar.

F.M. Wiest USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - F.M. Wiest USA, Inc.

12 devices

1-12 of 12

Cleared Dec 15, 1994

HYSTEROMAT(TM) 3700

K921871 · HIG

Obstetrics & Gynecology · 969d

Cleared Feb 17, 1993

CAMSYS 6300

K920574 · EXQ

Gastroenterology & Urology · 376d

Cleared Jul 23, 1992

MERKUR 4000

K920575 · FAP

Gastroenterology & Urology · 167d

Cleared Apr 24, 1992

URETEROMAT 4400

K915751 · EZN

Gastroenterology & Urology · 123d

Cleared Nov 21, 1991

HYSTEROFLATOR 1500

K911844 · HIG

Obstetrics & Gynecology · 210d

Cleared Jul 09, 1991

SPACE(TM) 7500

K912071 · IKN

Gastroenterology & Urology · 60d

Cleared Mar 29, 1991

LAPAROFLATOR ELECTRONIC 3509

K910883 · HIF

Obstetrics & Gynecology · 28d

Cleared Mar 02, 1988

LAPAROFLATOR 3000, STANDARD AND ELECTRONIC

K875137 · HES

Obstetrics & Gynecology · 78d

F.M. WEIST,KG (URODYNAMIC SYSTEMS)

K860571 · FAP

Gastroenterology & Urology · 32d

F.M. Wiest USA, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - F.M. Wiest USA, Inc.

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