510(k) K884852 ยท HCC Device, Biofeedback
BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.
| Applicant | Moe, Soquel CA, US |
| Decision | Substantially Equivalent, Feb 2, 1989 |
| Received | Nov 18, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884852
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.