510(k) K092833 ยท EKX Handpiece, Direct Drive, Ac-Powered
ENDOMAX CORDLESS ENDODONTIC HANDPIECE
| Applicant | Dentamerica, City Of Industry CA, US |
| Decision | Substantially Equivalent, Jan 7, 2010 |
| Received | Sep 15, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092833
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.