510(k) K993482 ยท GIS Test, Fibrinogen
K-ASSAY FIBRINOGEN
| Applicant | Kamiya Biomedical Co., Seattle WA, US |
| Decision | Substantially Equivalent, Dec 6, 1999 |
| Received | Oct 14, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993482
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.