Leocor, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K924110 | LEOCOR CORFLO PUMP -- MODIFICATION | DQI | 1992-09-01 | View |
| 510(k) | K911270 | LEOCOR GUIDING CATHETER | DQO | 1992-01-17 | View |
| 510(k) | K900350 | LEOCOR CORFLO(TM) PUMP | DXK | 1990-07-17 | View |
No matching devices.
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