ClearanceBrief
510(k) K100248 ยท KIF Resin, Root Canal Filling

DRFP PROSMART ROOT CANAL OBTURATION SYSTEM, PROPOINTS 4% 6%, PT, S

ApplicantDrfp , Ltd., Amsterdam, Nh, NL
DecisionSubstantially Equivalent, Oct 22, 2010
ReceivedJan 27, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K100248

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.