510(k) K861973 ยท GHH Fibrin Split Products
D-DI TEST KIT
| Applicant | American Bioproducts Co., Parsippany NJ, US |
| Decision | Substantially Equivalent, Sep 4, 1986 |
| Received | May 21, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861973
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.