ClearanceBrief
510(k) K821438 ยท DRX Electrode, Electrocardiograph

RED DOT MONITORING ELECTRODES #2260/65

Applicant3M Company, White City OR, US
DecisionSubstantially Equivalent, May 25, 1982
ReceivedMay 13, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821438

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.