510(k) K132057 ยท GXY Electrode, Cutaneous
DYNATRON PELTIER THERMOSTIM PROBE
| Applicant | Dynatronics Corp., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jan 24, 2014 |
| Received | Jul 3, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132057
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.