510(k) K800319 ยท HCC Device, Biofeedback
ALPHA DETECTOR
| Applicant | M.O.E Electronics Research & Prod., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 3, 1980 |
| Received | Feb 12, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800319
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.