510(k) K202913 ยท GXY Electrode, Cutaneous
NeuroCap (Model DEC22)
| Applicant | Memory MD, Inc., Bohemia NY, US |
| Decision | Substantially Equivalent, Mar 5, 2021 |
| Received | Sep 29, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202913
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.