510(k) K781880 ยท GIS Test, Fibrinogen
ASSAY KIT, THROMBO-SCREEN
| Applicant | Pacific Hemostasis, Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 4, 1978 |
| Received | Nov 6, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781880
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.