510(k) K994341 ยท GFX Fibrinogen Standard
FIBRINOGEN CALIBRATOR KIT
| Applicant | Dade Behring, Inc., Newark DE, US |
| Decision | Substantially Equivalent, Mar 3, 2000 |
| Received | Dec 23, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994341
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.