510(k) K121702 ยท ILX Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE
| Applicant | Orthocor Medical, Ashland MA, US |
| Decision | Substantially Equivalent, May 6, 2013 |
| Received | Jun 8, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121702
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.