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F.M. Wiest USA, Inc.

FDA 510(k) & PMA Approved Devices — 12 products

Total Devices12
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K921871 HYSTEROMAT(TM) 3700HIG1994-12-15 View
510(k) K920574 CAMSYS 6300EXQ1993-02-17 View
510(k) K920575 MERKUR 4000FAP1992-07-23 View
510(k) K915751 URETEROMAT 4400EZN1992-04-24 View
510(k) K911844 HYSTEROFLATOR 1500HIG1991-11-21 View
510(k) K912071 SPACE(TM) 7500IKN1991-07-09 View
510(k) K910883 LAPAROFLATOR ELECTRONIC 3509HIF1991-03-29 View
510(k) K875137 LAPAROFLATOR 3000, STANDARD AND ELECTRONICHES1988-03-02 View
510(k) K871180 ARTHRO AUTOMAT 5002HRX1987-09-29 View
510(k) K871181 ARTHROCOMBI 5003HRX1987-09-29 View
510(k) K865066 ARTHROFLATORHRX1987-04-20 View
510(k) K860571 F.M. WEIST,KG (URODYNAMIC SYSTEMS)FAP1986-03-18 View
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