510(k) K202542 ยท KXP Stent, Vaginal
Allura Vaginal Stent
| Applicant | Pmt Corporation, Chanhassen MN, US |
| Decision | Substantially Equivalent, Sep 30, 2020 |
| Received | Sep 2, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202542
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.