Amgen, 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) | K894943 | CLINIGEN ERYTHROPOIETIN HUMAN SERUM CONTROLS 1,2,3 | GGT | 1989-10-10 | View |
| 510(k) | K882686 | ERYTHROPOIETIN ENZYME IMMUNOASSAY | GGT | 1988-12-20 | View |
No matching devices.
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