ClearanceBrief
510(k) K160746 ยท DPS Electrocardiograph

CARDIOLINE touchECG

ApplicantCardioline S.P.A, Z.I. Spini Di Gardolo, IT
DecisionSubstantially Equivalent, Nov 2, 2016
ReceivedMar 18, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160746

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.