ClearanceBrief
510(k) K062079 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

XENIUM DIALYZER, MODELS 110, 130, 150, 170, 190 AND 210

ApplicantBaxter Healthcare Corporation, Mcgaw Park IL, US
DecisionSubstantially Equivalent, Oct 19, 2006
ReceivedJul 21, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062079

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.