ClearanceBrief
510(k) K780081 ยท FKQ System, Dialysate Delivery, Central Multiple Patient

DIALYZING FLUIDE DELIVERY SYSTEM

ApplicantTravenol Laboratories, S.A., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 31, 1978
ReceivedJan 16, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780081

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.