ClearanceBrief
510(k) K212112 ยท DPS Electrocardiograph

Cardiologs Holter Platform

ApplicantCardiologs Technologies, Paris, FR
DecisionSubstantially Equivalent, Nov 18, 2021
ReceivedJul 6, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K212112

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.