ClearanceBrief
510(k) K874535 ยท DZI Drill, Bone, Powered

MICROTEK MINI-MAX DRILL SYSTEM

ApplicantMicrotek Medical, Inc., Columbus MS, US
DecisionSubstantially Equivalent, Nov 23, 1987
ReceivedNov 3, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874535

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.