ClearanceBrief
510(k) K940908 ยท DZP Instrument, Diamond, Dental

DUNHALL/OMNII INTERNATIONAL ROTARY DIAMOND BURS

ApplicantDunhall Pharmaceuticals, Inc., Gravette AR, US
DecisionSubstantially Equivalent, Aug 29, 1994
ReceivedFeb 24, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940908

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.