ClearanceBrief
510(k) K821739 ยท EKX Handpiece, Direct Drive, Ac-Powered

J. MORITA FLEX M-3 TORX HARDPIECE

ApplicantPacific Dental Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 25, 1982
ReceivedJun 14, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821739

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.