Retroperfusion Systems, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K902943 | RSI FEMORAL GUIDING CATHETER | DQO | 1990-10-03 | View |
| 510(k) | K865074 | CORDAY CORONARY SINUS INFUSION CATHETER | DQY | 1987-05-06 | View |
No matching devices.
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