ClearanceBrief
510(k) K812442 ยท FRN Pump, Infusion

3M INFUSION SYSTEM

Applicant3M Company, White City OR, US
DecisionSubstantially Equivalent, Sep 16, 1981
ReceivedAug 27, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812442

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.