510(k) K870793 ยท HCC Device, Biofeedback
SELF REGULATION SYS PROF SERIES BIOFEEDBACK DEVICE
| Applicant | Self Regulation Systems, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, May 1, 1987 |
| Received | Feb 26, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870793
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.