510(k) K092933 ยท EFB Handpiece, Air-Powered, Dental
SAF (SELF ADJUSTING FILE)
| Applicant | Redent-Nova , Ltd., Washington, D.C. DC, US |
| Decision | Substantially Equivalent, Jan 14, 2010 |
| Received | Sep 23, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092933
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.