510(k) K964718 ยท DAP Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control
STA D-DI CALIBRATOR KIT
| Applicant | American Bioproducts Co., Parisppany NJ, US |
| Decision | Substantially Equivalent, May 23, 1997 |
| Received | Nov 25, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964718
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.