ClearanceBrief
510(k) K811783 ยท FRN Pump, Infusion

ENDOPUMP

ApplicantMedtron Development , Ltd., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 11, 1981
ReceivedJun 23, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K811783

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.