510(k) K954737 ยท HCC Device, Biofeedback
SURFACE ELECTROMYOGRAPH BIOFEEDBACK MUSCLE ACTIVITY DEVICE
| Applicant | J-Tech, Inc., Alpine UT, US |
| Decision | Substantially Equivalent, Jul 3, 1996 |
| Received | Oct 16, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954737
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.