510(k) K910317 ยท MFD Cannula, Intrauterine Insemination
UNI-SEM(TM)
| Applicant | Unimar, Inc., Wilton CT, US |
| Decision | Substantially Equivalent, May 1, 1991 |
| Received | Jan 24, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910317
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.