ClearanceBrief
510(k) K103564 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

VENOFER PUMP

ApplicantRenal Solutions, Inc., Warrendale PA, US
DecisionSubstantially Equivalent, Feb 10, 2011
ReceivedDec 6, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K103564

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.