510(k) K191225 ยท GXY Electrode, Cutaneous
EEG Electrode Template
| Applicant | Rhythmlink International, LLC, Columbia SC, US |
| Decision | Substantially Equivalent, Aug 5, 2019 |
| Received | May 7, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191225
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.