510(k) K233548 · HHW Pessary, Vaginal
Uresta®
| Applicant | Resilia, Inc., Moncton, CA |
| Decision | Substantially Equivalent, Apr 3, 2024 |
| Received | Nov 3, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233548
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.