510(k) K940176 ยท MFD Cannula, Intrauterine Insemination
ACKRAD IUI SET FOR INTRAUTERINE INSEMINATION
| Applicant | Ackrad Laboratories, Cranford NJ, US |
| Decision | Substantially Equivalent, Apr 23, 1996 |
| Received | Jan 11, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940176
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.