ClearanceBrief
510(k) K932529 ยท EKS File, Pulp Canal, Endodontic

LIGHTSPEED DENTAL HAND INSTRUMENT

ApplicantLightspeed Endodontics, Houston TX, US
DecisionSubstantially Equivalent, Nov 4, 1993
ReceivedMay 25, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932529

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.