510(k) K162667 ยท MQF Catheter, Assisted Reproduction
Kitazato IUI Catheter
| Applicant | Kitazato Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, May 11, 2017 |
| Received | Sep 26, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162667
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.