510(k) K925750 ยท HCC Device, Biofeedback
RELAXOMAT
| Applicant | Relaxomat, Inc., Tampa FL, US |
| Decision | Substantially Equivalent, Jan 31, 1995 |
| Received | Nov 13, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925750
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.