ClearanceBrief
510(k) K830994 ยท KDN System, Perfusion, Kidney

REDOX CONTROLLER

ApplicantSt. Louis Univ. Medical Center, Walker MI, US
DecisionSubstantially Equivalent, May 27, 1983
ReceivedMar 29, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830994

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.