510(k) K861950 ยท HCC Device, Biofeedback
THE FM-212A BIOFEEDBACK UNIT
| Applicant | Hosa Technology, Inc., Cerritos CA, US |
| Decision | Substantially Equivalent, Apr 22, 1987 |
| Received | May 20, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861950
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.