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F.M. Wiest USA, Inc.

12 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
HYSTEROMAT(TM) 3700 (K921871)F.M. Wiest USA, Inc.1994-12-15
CAMSYS 6300 (K920574)F.M. Wiest USA, Inc.1993-02-17
MERKUR 4000 (K920575)F.M. Wiest USA, Inc.1992-07-23
URETEROMAT 4400 (K915751)F.M. Wiest USA, Inc.1992-04-24
HYSTEROFLATOR 1500 (K911844)F.M. Wiest USA, Inc.1991-11-21
SPACE(TM) 7500 (K912071)F.M. Wiest USA, Inc.1991-07-09
LAPAROFLATOR ELECTRONIC 3509 (K910883)F.M. Wiest USA, Inc.1991-03-29
LAPAROFLATOR 3000, STANDARD AND ELECTRONIC (K875137)F.M. Wiest USA, Inc.1988-03-02
ARTHROCOMBI 5003 (K871181)F.M. Wiest USA, Inc.1987-09-29
ARTHRO AUTOMAT 5002 (K871180)F.M. Wiest USA, Inc.1987-09-29
ARTHROFLATOR (K865066)F.M. Wiest USA, Inc.1987-04-20
F.M. WEIST,KG (URODYNAMIC SYSTEMS) (K860571)F.M. Wiest USA, Inc.1986-03-18

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