510(k) K973537 ยท HCC Device, Biofeedback
PATHWAY ELECTROMYOGRAPH
| Applicant | The Prometheus Group, Duxbury MA, US |
| Decision | Substantially Equivalent, Dec 17, 1997 |
| Received | Sep 18, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973537
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.