510(k) K242326 ยท GXY Electrode, Cutaneous
Wave Electrode (AE02-60); Wave Electrode (AE02-50)
| Applicant | Bionit Labs Srl, Soleto, IT |
| Decision | Substantially Equivalent, Jan 2, 2025 |
| Received | Aug 6, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242326
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.