510(k) K880077 ยท GHH Fibrin Split Products
FIBRINOSTICON
| Applicant | Organon Teknika Corp., Durham NC, US |
| Decision | Substantially Equivalent, Feb 9, 1988 |
| Received | Jan 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880077
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.