510(k) K962671 ยท GJT Plasma, Coagulation Factor Deficient
STA-VWF CALIBRATOR KIT
| Applicant | American Bioproducts Co., Parisppany NJ, US |
| Decision | Substantially Equivalent, Sep 13, 1996 |
| Received | Jul 9, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962671
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.