510(k) K850849 ยท HCC Device, Biofeedback
MYOMETER EMG BIOFEEDBACK DEVICE
| Applicant | Physio Technology, Inc., Topeka KS, US |
| Decision | Substantially Equivalent, May 31, 1985 |
| Received | Mar 1, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850849
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.