510(k) K234061 ยท KPI Stimulator, Electrical, Non-Implantable, For Incontinence
StarFormer
| Applicant | Fotona D.O.O., Ljubljana, SI |
| Decision | Substantially Equivalent, Jul 1, 2024 |
| Received | Dec 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234061
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.