Schneider-Shilley (USA)
Minneapolis, MN, US
Schneider-Shilley (Usa) appears in FDA device records in Minneapolis, MN. FDA records list 9 510(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
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Schneider-Shilley (USA) between 1988 and 1989. The busiest year on record is 1988, with 8. The most recent is 1989, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 8 |
| 1989 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K882826 | SOFTRAC-PTA PERIPHERAL DILATATION CATHETER | LIT | Substantially Equivalent | |
| K875175 | MODIFIED PERIPHERAL DILATATION CATHETERS | LIT | Substantially Equivalent | |
| K881197 | SOFTRAC-PTA(TM) PERIPHERAL DILATATION CATHETER | LIT | Substantially Equivalent | |
| K875323 | MODIFIED SCHNEIDER-SHILEY WIRE TORQUER | DQX | Substantially Equivalent | |
| K875322 | MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER | KRK | Substantially Equivalent | |
| K875327 | MODIFIED SELDINGER INITIAL PUNCTURE INSTRUMENT | DRE | Substantially Equivalent | |
| K875324 | MODIFIED SCHNEIDER SHILEY INFLATION SYRINGES | DXT | Substantially Equivalent | |
| K875326 | MODIFIED SCHNEIDER-SHILEY FLUSHING CATHETER | DQO | Substantially Equivalent | |
| K875325 | MODIFIED OCCLUDER/FLUSHING CATHETER STOPCOCK | DQO | 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