ClearanceBrief
510(k) K964755 ยท KOJ Airbrush

MICROJET CAVITY PREPARATION SYSTEM

ApplicantMidwest Dental Products Corp., Des Plaines IL, US
DecisionSubstantially Equivalent, Sep 11, 1997
ReceivedNov 27, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964755

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.