Micor, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K031600 | CONDUCTION CATHETER | FRN | 2003-08-13 | View |
| 510(k) | K003966 | WUNDCATH CONDUCTION CATHETER | FRN | 2001-07-17 | View |
| 510(k) | K001717 | MICOR CONDUCTION CATHETER | BSO | 2000-09-20 | View |
| 510(k) | K001940 | MICOR ANESTHESIA CONDUCTION KIT | CAZ | 2000-08-11 | View |
| 510(k) | K991879 | SPRING-WOUND EPIDURAL CATHETER | BSO | 1999-10-28 | View |
| 510(k) | K861008 | PERCUTANEOUS CATHETERS | DQY | 1986-04-29 | View |
| 510(k) | K860339 | PERCUTANEOUS CATHETERS | DQY | 1986-03-31 | View |
| 510(k) | K854018 | ANGIOGRAPHY CATHETERS | DQO | 1986-01-16 | View |
No matching devices.
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