510(k) K091791 ยท ILX Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
PROVANT SYSTEM, MODEL 4201
| Applicant | Regenesis Biomedical, Inc., Scottsdale AZ, US |
| Decision | Substantially Equivalent, Apr 7, 2010 |
| Received | Jun 17, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091791
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.