510(k) K914920 ยท HCC Device, Biofeedback
BIOFEEDBACK SYSTEM/3
| Applicant | Davicon, Inc., Attleboro MA, US |
| Decision | Substantially Equivalent, Nov 16, 1992 |
| Received | Nov 4, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914920
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.