ClearanceBrief
510(k) K803290 ยท DZI Drill, Bone, Powered

ARTUS DRILL #3000

ApplicantJedmed Instrument Co., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 28, 1981
ReceivedDec 30, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K803290

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.