510(k) K141666 ยท MQF Catheter, Assisted Reproduction
FERTILIGENT SLOW RELEASE IUI CATHETER KIT
| Applicant | Fertiligent, Ltd., Indianapolis IN, US |
| Decision | Substantially Equivalent, Feb 3, 2015 |
| Received | Jun 23, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141666
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.