ClearanceBrief
510(k) K912589 ยท FRN Pump, Infusion

AVI MODEL 840D DUAL CHANNEL INFUSION PUMP

Applicant3M Avi, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Oct 17, 1991
ReceivedJun 10, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912589

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.