ClearanceBrief
510(k) K100600 ยท EKX Handpiece, Direct Drive, Ac-Powered

PROSTHODONTIC SCREWDRIVER , MODEL IA-400

ApplicantW&H Dentalwerk Buermoos GmbH, Buermoos, AT
DecisionSubstantially Equivalent, Jul 9, 2010
ReceivedMar 3, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K100600

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.