510(k) K897178 ยท KQX Goniometer, Ac-Powered
DYNATRON 360 RANGE OF MOTION TESTING DEVICE
| Applicant | Dynatronics Corp., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Apr 18, 1990 |
| Received | Dec 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K897178
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.