ClearanceBrief
510(k) K820859 ยท LBW Set, Dialysis, Single Needle (Co-Axial Flow)

COAXIAL DUAL FLOW CATHETER

ApplicantTerumo Medical Corp., Elkton MD, US
DecisionSubstantially Equivalent, Apr 16, 1982
ReceivedMar 29, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820859

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.