ClearanceBrief
510(k) K792229 ยท DPS Electrocardiograph

ELECTROCARDIOGRAPH, MODEL ECG-5151

ApplicantNihon Kohden America, Inc., Foothill CA, US
DecisionSubstantially Equivalent, Nov 21, 1979
ReceivedNov 5, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792229

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.