510(k) K894840 ยท HCC Device, Biofeedback
MYODAC2 BIOFEEDBACK DEVICE
| Applicant | Thought Technology , Ltd., Montreal, Quebec, CA |
| Decision | Substantially Equivalent, Oct 13, 1989 |
| Received | Jul 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894840
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.