ClearanceBrief
510(k) K896361 ยท EFB Handpiece, Air-Powered, Dental

HANDPIECE FIBER OPTIC SYSTEM IMPROVEMENT FEATURE

ApplicantDentalez Group, Lancaster PA, US
DecisionSubstantially Equivalent, Feb 2, 1990
ReceivedNov 6, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896361

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.