510(k) K192823 ยท GWF Stimulator, Electrical, Evoked Response
MEGA-TMS
| Applicant | Soterix Medical, Inc., New York NY, US |
| Decision | Substantially Equivalent, Aug 13, 2021 |
| Received | Oct 2, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192823
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.