510(k) K092579 ยท MQF Catheter, Assisted Reproduction
INTRAUTERINE INSEMINATION (IUI) CATHETER
| Applicant | Fertiligent, Ltd., Indianapolis IN, US |
| Decision | Substantially Equivalent, Apr 2, 2010 |
| Received | Aug 17, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092579
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.