ClearanceBrief
510(k) K992584 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)

PE 501 PC-ECG MONITOR

ApplicantNhe Corp., Richmond VA, US
DecisionSubstantially Equivalent, Jan 13, 2000
ReceivedAug 2, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992584

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.