ClearanceBrief
510(k) K962877 ยท EFB Handpiece, Air-Powered, Dental

MIDWEST 300 SE

ApplicantMidwest Dental Products Corp., Des Plaines IL, US
DecisionSubstantially Equivalent, Oct 18, 1996
ReceivedJul 24, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962877

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.