ClearanceBrief
510(k) K900018 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

HOLLOW FIBER DIALYZER, BIO CARE PS 130

ApplicantNational Medical Care, Medical Products Div., Inc., Rockleigh NJ, US
DecisionSubstantially Equivalent, Jul 27, 1990
ReceivedJan 2, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900018

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.