510(k) K875308 ยท HCC Device, Biofeedback
PROFESSIONAL SERIES BIOFEEDBACK DEVICES MODEL 421
| Applicant | Self Regulation Systems, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Feb 26, 1988 |
| Received | Dec 29, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875308
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.