F.M. Wiest USA, Inc.
Cherry Hill, NJ, US
F.M. Wiest USA, Inc. appears in FDA device records in Cherry Hill, NJ. FDA records list 12 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for F.M. Wiest USA, Inc. between 1986 and 1994. The busiest year on record is 1987, with 3. The most recent is 1994, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1986 | 1 |
| 1987 | 3 |
| 1988 | 1 |
| 1991 | 3 |
| 1992 | 2 |
| 1993 | 1 |
| 1994 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K921871 | HYSTEROMAT(TM) 3700 | HIG | Substantially Equivalent | |
| K920574 | CAMSYS 6300 | EXQ | Substantially Equivalent | |
| K920575 | MERKUR 4000 | FAP | Substantially Equivalent | |
| K915751 | URETEROMAT 4400 | EZN | Substantially Equivalent | |
| K911844 | HYSTEROFLATOR 1500 | HIG | Substantially Equivalent | |
| K912071 | SPACE(TM) 7500 | IKN | Substantially Equivalent | |
| K910883 | LAPAROFLATOR ELECTRONIC 3509 | HIF | Substantially Equivalent | |
| K875137 | LAPAROFLATOR 3000, STANDARD AND ELECTRONIC | HES | Substantially Equivalent | |
| K871181 | ARTHROCOMBI 5003 | HRX | Substantially Equivalent | |
| K871180 | ARTHRO AUTOMAT 5002 | HRX | Substantially Equivalent | |
| K865066 | ARTHROFLATOR | HRX | Substantially Equivalent | |
| K860571 | F.M. WEIST,KG (URODYNAMIC SYSTEMS) | FAP | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain