510(k) K900639 ยท HCC Device, Biofeedback
DYNATRON 350 EMG/BIOFEEDBACK ANALYZER
| Applicant | Dynatronics Laser Corp., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Oct 4, 1990 |
| Received | Feb 9, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900639
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.