ClearanceBrief
510(k) K791540 ยท DPS Electrocardiograph

ELECTROCARDIOGRAPH MODEL ECG-5403

ApplicantNihon Kohden America, Inc., Foothill CA, US
DecisionSubstantially Equivalent, Sep 4, 1979
ReceivedAug 10, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791540

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.