510(k) K884848 ยท HCC Device, Biofeedback
BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV
| 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 K884848
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.