ClearanceBrief
510(k) K060661 ยท DRX Electrode, Electrocardiograph

MACTRODE 3

ApplicantGe Medical Systems Information Technologies, Milwaukee WI, US
DecisionSubstantially Equivalent, Apr 7, 2006
ReceivedMar 13, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K060661

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.