Lafayette Pharmacal, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K931896 | PRO-FLO SYSTEM | FCE | 1993-08-26 | View |
| 510(k) | K884379 | MAGLINTE ENTEROCLYSIS CATHETER | FGD | 1989-02-28 | View |
| 510(k) | K881609 | SITZMARKS | FFX | 1988-07-08 | View |
| 510(k) | K860441 | ENTROKIT WITH MAGLINTE CATHETER | KGC | 1986-03-12 | View |
No matching devices.
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