510(k) K210764 ยท HIR Perineometer
Flyte
| Applicant | Pelvital USA, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 13, 2021 |
| Received | Mar 15, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K210764
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.