510(k) K961718 ยท HCC Device, Biofeedback
DEI MODEL 20 EEG
| Applicant | Discovery Engineering Intl., Inc., Topeka KS, US |
| Decision | Substantially Equivalent, Aug 27, 1996 |
| Received | May 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961718
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.