510(k) K897132 ยท HCC Device, Biofeedback
PATHWAY II ELECTROMYOGRAPH
| Applicant | The Prometheus Group, Portsmouth NH, US |
| Decision | Substantially Equivalent, Apr 18, 1991 |
| Received | Dec 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K897132
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.