510(k) K990739 ยท EKX Handpiece, Direct Drive, Ac-Powered
QUANTEC-E ENDO SYSTEM
| Applicant | Sybron Dental Specialties, Inc., Orange CA, US |
| Decision | Substantially Equivalent, May 26, 1999 |
| Received | Mar 5, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990739
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.