510(k) K162460 · GXY Electrode, Cutaneous
WAVi Headset and WAVi eSoc Single Use Electrode Contacts
| Applicant | Wavi Co., Englewood CO, US |
| Decision | Substantially Equivalent, Apr 28, 2017 |
| Received | Sep 2, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162460
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.