ClearanceBrief
510(k) K860569 ยท EKR Plugger, Root Canal, Endodontic

ENDODONTIC ROOT CANAL PLUGGER

ApplicantDentsply Intl., York PA, US
DecisionSubstantially Equivalent, Mar 26, 1986
ReceivedFeb 11, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860569

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.