510(k) K905764 ยท MFD Cannula, Intrauterine Insemination
SEMINOR
| Applicant | Promedex, Inc., Fort Woth TX, US |
| Decision | Substantially Equivalent, Mar 12, 1991 |
| Received | Dec 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905764
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.