ClearanceBrief
510(k) K022909 ยท DRX Electrode, Electrocardiograph

NIKOMED TRACE 1 ECG ELECTRODES

ApplicantNikomed U.S.A., Inc., Stillwater MN, US
DecisionSubstantially Equivalent, Jan 9, 2003
ReceivedSep 3, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K022909

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.