510(k) K120835 ยท GXY Electrode, Cutaneous
DYNATRON THERMOSTIM PROBE-DONE
| Applicant | Dynatronics Corporation, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Aug 20, 2012 |
| Received | Mar 20, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120835
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.