ClearanceBrief
510(k) K171942 ยท DPS Electrocardiograph

Electrocardiograph

ApplicantEdan Instruments, Inc., Shenzhen, CN
DecisionSubstantially Equivalent, Jan 24, 2018
ReceivedJun 28, 2017
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K171942

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.