ClearanceBrief
510(k) K992380 ยท EFB Handpiece, Air-Powered, Dental

ENDO-EZE MOTOR AND HANDPIECE

ApplicantUltradent Products, Inc., South Jordan UT, US
DecisionSubstantially Equivalent, Oct 13, 1999
ReceivedJul 16, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992380

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.