510(k) K960762 ยท HCC Device, Biofeedback
SYNERGY PLUS
| Applicant | The Prometheus Group, Duxbury MA, US |
| Decision | Substantially Equivalent, Jun 13, 1996 |
| Received | Feb 26, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960762
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.