510(k) K951213 ยท HCC Device, Biofeedback
RELAXPLUS
| Applicant | Ultramind International , Ltd., Eilat, IL |
| Decision | Substantially Equivalent, Sep 20, 1995 |
| Received | Mar 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951213
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.