510(k) K963031 ยท MFD Cannula, Intrauterine Insemination
GENXCATHETER
| Applicant | Genx Intl., Inc., Madison CT, US |
| Decision | Substantially Equivalent, Oct 21, 1996 |
| Received | Aug 5, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963031
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.