510(k) K122879 ยท HCC Device, Biofeedback
EEGER4 MODEL 4.3
| Applicant | Eeg Software, LLC, Northridge CA, US |
| Decision | Substantially Equivalent, Feb 6, 2013 |
| Received | Sep 19, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122879
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.