510(k) K792659 ยท HCC Device, Biofeedback
FEEDBACK EDR SYSTEM MODEL ME-1
| Applicant | Bio-Feedback Systems, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 9, 1980 |
| Received | Dec 26, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792659
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.