510(k) K222404 · GZL Electrode, Depth
Evo® sEEG System
| Applicant | Neuroone Medical Technologies Corp., Eden Prairie MN, US |
| Decision | Substantially Equivalent, Oct 20, 2022 |
| Received | Aug 9, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222404
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.