510(k) K242525 · KOI Stimulator, Nerve, Peripheral, Electric
iTOF®
| Applicant | Nerbio Medical Software Platforms, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Dec 5, 2024 |
| Received | Aug 26, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242525
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.