510(k) K812628 ยท GFX Fibrinogen Standard
ACA FIBRINOGEN CALIBRATOR
| Applicant | E.I. Dupont DE Nemours & Co., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 24, 1981 |
| Received | Sep 15, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812628
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.