ClearanceBrief
510(k) K832662 ยท KXR Applicator, Resin

DENTAL SYRINGE SYSTEM-VARIOUS STYLES

ApplicantCentrix, Inc., Walker MI, US
DecisionSubstantially Equivalent, Oct 4, 1983
ReceivedAug 8, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832662

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.