510(k) K884850 ยท HCC Device, Biofeedback
BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30
| 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 K884850
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.