510(k) K861417 ยท GGP Test, Qualitative And Quantitative Factor Deficiency
ASSERA-PLATE VWF KIT
| Applicant | American Bioproducts Co., Parsippany NJ, US |
| Decision | Substantially Equivalent, Jun 25, 1986 |
| Received | Apr 15, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861417
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.