ClearanceBrief
510(k) K855251 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

MODIFICATION ASAHI NEW PAN-SERIES HEMOFILTERS

ApplicantAdvocacy International, Ltd., Washington DC, US
DecisionSubstantially Equivalent, Feb 4, 1986
ReceivedDec 30, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K855251

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.