ClearanceBrief
510(k) K801677 ยท DPS Electrocardiograph

ELECTROCARDIOGRAPH, MODEL ECG-5503

ApplicantNihon Kohden America, Inc., Foothill CA, US
DecisionSubstantially Equivalent, Aug 7, 1980
ReceivedJul 22, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801677

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.