Kabi Pharmacia, 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) | K923832 | PHARMACIA CAP SYSTEM IGE FEIA -- MODIFICATION | DGC | 1992-11-25 | View |
| 510(k) | K915083 | COAMATE(R) ANTITHROMBIN CHROMOGENIC ASSAY | JBQ | 1992-01-03 | View |
No matching devices.
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