510(k) K072304 ยท GFX Fibrinogen Standard
FIBRINOGEN CALIBRATOR KIT
| Applicant | Dade Behring, Inc., Newark DE, US |
| Decision | Substantially Equivalent, Sep 19, 2007 |
| Received | Aug 17, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072304
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.