510(k) K070931 ยท ILX Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
MODEL PMT850
| Applicant | Promedtek, Inc., Washington DC, US |
| Decision | Substantially Equivalent, May 24, 2007 |
| Received | Apr 3, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070931
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.