510(k) K852963 ยท HCC Device, Biofeedback
MYO-ACTUATOR
| Applicant | Verimed Holdings, Inc., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Jan 21, 1986 |
| Received | Jul 12, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852963
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.