510(k) K925197 ยท HCC Device, Biofeedback
PSI 220 DUAL EMG
| Applicant | Fasstech, Burlington MA, US |
| Decision | Substantially Equivalent, Feb 2, 1993 |
| Received | Oct 15, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925197
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.