510(k) K852512 ยท GHH Fibrin Split Products
THROMBO SCREEEN FIBRIN DEGRADATION PRODUCT KIT
| Applicant | Pacific Hemostasis, Ventura CA, US |
| Decision | Substantially Equivalent, Sep 17, 1985 |
| Received | Jun 12, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852512
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.