510(k) K832714 ยท HCC Device, Biofeedback
VERIMED MYOEXORCISER
| Applicant | Verimed Holdings, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 28, 1983 |
| Received | Aug 12, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832714
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.