510(k) K963571 ยท FMI Needle, Hypodermic, Single Lumen
VYGON MULTI-DOSE VIAL ADAPTER & BIONECTOR
| Applicant | Vygon Corp., West Cadwell NJ, US |
| Decision | Substantially Equivalent, Jun 2, 1997 |
| Received | Sep 5, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963571
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.