ClearanceBrief
510(k) K897013 ยท FRN Pump, Infusion

AVI MICRO 210CM INFUSION PUMP

Applicant3M Company, St. Paul MN, US
DecisionSubstantially Equivalent, Mar 8, 1990
ReceivedDec 19, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K897013

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.