ClearanceBrief
510(k) K822582 ยท DPS Electrocardiograph

QUIKPAGE SCANNER

ApplicantAgilent Technologies, Walker MI, US
DecisionSubstantially Equivalent, Sep 21, 1982
ReceivedAug 25, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822582

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.