510(k) K983045 ยท KXP Stent, Vaginal
AMIELLE
| Applicant | Owen Mumford USA, Inc., Marietta GA, US |
| Decision | Substantially Equivalent, Nov 25, 1998 |
| Received | Sep 1, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983045
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.