510(k) K091913 ยท EKX Handpiece, Direct Drive, Ac-Powered
HI TECH IMPLANT, HT PHYSIO IMPLANT
| Applicant | By Dental Srl, Serravalle Poli; Pistoia, IT |
| Decision | Substantially Equivalent, Oct 30, 2009 |
| Received | Jun 30, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091913
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.