510(k) K110223 ยท GXY Electrode, Cutaneous
WAVEGUARD (TM) EEG CAP
| Applicant | Eemagine Medical Imaging Solutions GmbH, Naples FL, US |
| Decision | Substantially Equivalent, Jun 29, 2011 |
| Received | Jan 25, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110223
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.