ClearanceBrief
510(k) K042822 ยท EKX Handpiece, Direct Drive, Ac-Powered

TCM ENDO V, MODEL 1534

ApplicantNOUVAG AG, Gebenstorf, CH
DecisionSubstantially Equivalent, Dec 22, 2004
ReceivedOct 12, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042822

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.