ClearanceBrief
510(k) K820014 ยท DPS Electrocardiograph

HOLTER ECG SCANNER

ApplicantLaser Scan Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 21, 1982
ReceivedJan 5, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820014

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.