510(k) K823511 ยท HCC Device, Biofeedback
EMG BIOFEEDBACK DEVICE
| Applicant | Nemectron Medical, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Mar 31, 1983 |
| Received | Nov 29, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823511
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.