510(k) K013501 ยท MQF Catheter, Assisted Reproduction
IUI, MODEL 4220; SMOOZE, MODEL 4225, L; SEMINOR, MODEL 4502 A, B
| Applicant | Gynetics Medical Products NV, Irvine CA, US |
| Decision | Substantially Equivalent, Nov 30, 2001 |
| Received | Oct 22, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013501
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.