F M Wiest Usa Inc

FDA Filings

This page includes the latest FDA filings for F M Wiest Usa Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

FDA Filings

Device
Company
DeviceDate
F.M. WIEST USA, INC.
HYSTEROMAT(TM) 37001994-12-15
F.M. WIEST USA, INC.
CAMSYS 63001993-02-17
F.M. WIEST USA, INC.
MERKUR 40001992-07-23
F.M. WIEST USA, INC.
URETEROMAT 44001992-04-24
F.M. WIEST USA, INC.
HYSTEROFLATOR 15001991-11-21
F.M. WIEST USA, INC.
SPACE(TM) 75001991-07-09
F.M. WIEST USA, INC.
LAPAROFLATOR ELECTRONIC 35091991-03-29
F.M. WIEST USA, INC.
LAPAROFLATOR 3000, STANDARD AND ELECTRONIC1988-03-02
F.M. WIEST USA, INC.
ARTHROCOMBI 50031987-09-29
F.M. WIEST USA, INC.
ARTHRO AUTOMAT 50021987-09-29
F.M. WIEST USA, INC.
ARTHROFLATOR1987-04-20
F.M. WIEST USA, INC.
F.M. WEIST,KG (URODYNAMIC SYSTEMS)1986-03-18

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