ClearanceBrief
510(k) K121409 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

ASAHI REXEED-SX/LX SERIES DIALYZER

ApplicantAsahi Kasei Medical Co., Ltd., Charlestown NH, US
DecisionSubstantially Equivalent, Feb 6, 2013
ReceivedMay 11, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121409

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.