510(k) K852176 ยท GHH Fibrin Split Products
DUPONT ACA FIBRIN OGEN DEGRAD-PRODUCTS CALIBRATOR
| Applicant | E.I. Dupont DE Nemours & Co., Inc., Wilmington DE, US |
| Decision | Substantially Equivalent, Aug 12, 1985 |
| Received | May 20, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852176
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.