510(k) K951969 ยท HCC Device, Biofeedback
MYOEXORCISER II FUAL
| Applicant | Verimed Holdings, Inc., Coral Springs FL, US |
| Decision | Substantially Equivalent, Jun 14, 1995 |
| Received | Apr 27, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951969
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.