510(k) K925988 ยท KQJ System, Fibrinogen Determination
MULTIFIBREN
| Applicant | Behring Diagnostics, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, Mar 1, 1993 |
| Received | Nov 25, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925988
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.