510(k) K890399 ยท GHH Fibrin Split Products
MODIFIED D-DI-TEST KIT
| Applicant | American Bioproducts Co., Parsippany NJ, US |
| Decision | Substantially Equivalent, Feb 7, 1989 |
| Received | Jan 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890399
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.