510(k) K761350 ยท HCC Device, Biofeedback
MYOTRON
| Applicant | Somatronics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 15, 1977 |
| Received | Dec 28, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K761350
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.