ClearanceBrief
510(k) K051534 ยท DPS Electrocardiograph

CARDIOLINE AR 600, AR 1200, AR 2100

ApplicantEt Medical Devices Spa, Cavareno, IT
DecisionSubstantially Equivalent, Oct 5, 2005
ReceivedJun 10, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K051534

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.