510(k) K921518 ยท MFD Cannula, Intrauterine Insemination
LIFETEK IUI CATHETER
| Applicant | Lifetek Medical, Inc., Deforest WI, US |
| Decision | Substantially Equivalent, May 10, 1994 |
| Received | Mar 31, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921518
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.