510(k) K200409 ยท HIR Perineometer
Pelvital System
| Applicant | Pelvital USA, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 10, 2020 |
| Received | Feb 19, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200409
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.