ClearanceBrief
510(k) K033559 ยท DRX Electrode, Electrocardiograph

12-LEAD GLOVE

ApplicantIneedmd, Stamford CT, US
DecisionSubstantially Equivalent, Dec 22, 2004
ReceivedNov 12, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033559

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.