510(k) K111623 ยท EBW Controller, Foot, Handpiece And Cord
I-ENDO DUAL
| Applicant | Satelec - Acteon Group, Mt. Laurel NJ, US |
| Decision | Substantially Equivalent, Jan 10, 2012 |
| Received | Jun 10, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111623
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.