510(k) K162240 ยท IMJ Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat
ProMedTek Model C1400 Shortwave Diathermy Device
| Applicant | Promedtek, Inc., Scottsdale AZ, US |
| Decision | Substantially Equivalent, Nov 17, 2016 |
| Received | Aug 9, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162240
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.