ClearanceBrief
510(k) K854011 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

RENALFO HEMOFILTER CAVHD

ApplicantRenal Systems, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Nov 5, 1985
ReceivedSep 30, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854011

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.