ClearanceBrief
510(k) K801303 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

MODEL 90 PRESSURE/CONDUCTIVITY/TEMP TEST

ApplicantWestern Laboratories Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 28, 1980
ReceivedJun 3, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801303

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.