510(k) K896052 ยท KQJ System, Fibrinogen Determination
FIBRINOGEN ASSAY KIT
| Applicant | Medical Diagnostic Technologies, Inc., Ventura CA, US |
| Decision | Substantially Equivalent, Nov 9, 1989 |
| Received | Oct 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896052
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.