F.M. Wiest USA, Inc.
12 FDA 510(k) clearances · Manufacturer
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| 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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