ClearanceBrief
510(k) K133488 ยท DZI Drill, Bone, Powered

PIEZOMED

ApplicantW&H Dentalwerk Buermoos GmbH, Burmoos, AT
DecisionSubstantially Equivalent, Oct 16, 2014
ReceivedNov 13, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133488

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.