510(k) K212655 ยท HIR Perineometer
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| Applicant | Pelvital USA, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 21, 2021 |
| Received | Aug 23, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K212655
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.