Novoste Corp.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K942977 | NOVOSTE PULSE PLUS BLOOD CONTAINMENT DEVICE | DYB | 1995-12-28 | View |
| 510(k) | K911527 | NOVOSTE GUIDING CATHETER | DQY | 1991-04-24 | View |
| 510(k) | K900460 | MODIFIED NOVOSTE ANGIOGRAPHIC CATHETER | DQO | 1990-07-17 | View |
| 510(k) | K896690 | MODIFIED ANGIOGRAPHIC CATHETER | DQO | 1990-01-24 | View |
| 510(k) | K875127 | NOVOSTE 4, 4.2, 5 AND 6 FRENCH CATHETERS | DQO | 1988-08-09 | View |
No matching devices.
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