ClearanceBrief
510(k) K210140 ยท DPS Electrocardiograph

electrocardiograph: SE-1202

ApplicantEdan Instruments, Inc., Shenzhen, CN
DecisionSubstantially Equivalent, Oct 1, 2021
ReceivedJan 19, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K210140

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.