510(k) K892649 ยท HCC Device, Biofeedback
VERIMED MYOEXORCISER III (MYO III)
| Applicant | Verimed Holdings, Inc., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Dec 13, 1989 |
| Received | Apr 12, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892649
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.