ClearanceBrief
510(k) K842225 ยท FKQ System, Dialysate Delivery, Central Multiple Patient

HEMODIAL CONCENTRATE MIXING APPARATUS

ApplicantLmf Medical Research & Manufacturing, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 2, 1984
ReceivedJun 5, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842225

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.