510(k) K861217 ยท GGP Test, Qualitative And Quantitative Factor Deficiency
VWF-IX:AG CONTROL PLASMA
| Applicant | American Bioproducts Co., Parsippany NJ, US |
| Decision | Substantially Equivalent, May 20, 1986 |
| Received | Mar 31, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861217
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.