ClearanceBrief
510(k) K232823 ยท DPS Electrocardiograph

MCG-S (AM1000)

ApplicantAmcg Co., Ltd., Seoul, KR
DecisionSubstantially Equivalent, Apr 5, 2024
ReceivedSep 13, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232823

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.