510(k) K834571 ยท KQJ System, Fibrinogen Determination
FIBRINOGEN TEST
| Applicant | Diatech, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 4, 1984 |
| Received | Dec 29, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834571
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.