Amgen, Inc. · Class II · Cleared Oct 10, 1989
| K-number | K894943 |
| Device name | CLINIGEN ERYTHROPOIETIN HUMAN SERUM CONTROLS 1,2,3 |
| Applicant | Amgen, Inc. |
| Product code | GGT |
| Device class | Class II |
| Decision date | Oct 10, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 864.7250 |
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