510(k) K943787 ยท DAP Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control
AURATEK FDP
| Applicant | Organon Teknika Corp., Durham NC, US |
| Decision | Substantially Equivalent, Sep 20, 1994 |
| Received | Aug 3, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943787
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.