510(k) K924892 ยท DAT Fibrinogen And Split Products, Peroxidase, Antigen, Antiserum, Control
FIBRINOSTIKA(R) FGDP MICROELISA SYSTEM
| Applicant | Organon Teknika Corp., Durham NC, US |
| Decision | Substantially Equivalent, Apr 21, 1994 |
| Received | Sep 29, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924892
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.