510(k) K050612 ยท EKX Handpiece, Direct Drive, Ac-Powered
LIGHTSPEED CORDLESS ENDODONTIC HANDPIECE
| Applicant | Lightspeed Technology, Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, May 4, 2005 |
| Received | Mar 10, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050612
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.