ClearanceBrief
510(k) K033597 ยท EKX Handpiece, Direct Drive, Ac-Powered

ATR 5000, LC 5000, IMPLANT SYSTEM

ApplicantAdvanced Technology Research (A.T.R.) S.R.L., Pistoia, IT
DecisionSubstantially Equivalent, Nov 25, 2003
ReceivedNov 14, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033597

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.