ClearanceBrief
510(k) K000710 ยท EFB Handpiece, Air-Powered, Dental

MD 10, SEM, SM 12, CBM

ApplicantNOUVAG AG, Kaufbeuren, DE
DecisionSubstantially Equivalent, May 11, 2000
ReceivedMar 2, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K000710

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.