510(k) K243339 ยท KOI Stimulator, Nerve, Peripheral, Electric
WiTOF
| Applicant | Idmed, Marseille, FR |
| Decision | Substantially Equivalent, Jun 23, 2025 |
| Received | Oct 25, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243339
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.