Medical Device Manufacturer · US , Cherry Hill , NJ

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

12 submissions · 12 cleared · Since 1986

12

Total

12

Cleared

0

Denied

FDA 510(k) Regulatory Record - F.M. Wiest USA, Inc. Obstetrics & Gynecology ✕

4 devices

1-4 of 4

Cleared Dec 15, 1994

HYSTEROMAT(TM) 3700

Obstetrics & Gynecology · 969d

Cleared Nov 21, 1991

HYSTEROFLATOR 1500

Obstetrics & Gynecology · 210d

Cleared Mar 29, 1991

LAPAROFLATOR ELECTRONIC 3509

Obstetrics & Gynecology · 28d

Cleared Mar 02, 1988

LAPAROFLATOR 3000, STANDARD AND ELECTRONIC

Obstetrics & Gynecology · 78d