510(k) K031540 ยท EKX Handpiece, Direct Drive, Ac-Powered
APEX ELECTRIC HANDPIECE SYSTEM
| Applicant | Lares Research, Inc., Chico CA, US |
| Decision | Substantially Equivalent, Jun 30, 2003 |
| Received | May 16, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031540
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.