510(k) K252334 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
PELVIPOWER Pelvic Functional Magnetic Stimulation (PELVIPOWER PelvicFMS) (033-0-1100-02)
| Applicant | Pontemedag, Arbon, CH |
| Decision | Substantially Equivalent, Apr 17, 2026 |
| Received | Jul 28, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252334
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.