ClearanceBrief
510(k) K131819 ยท DPS Electrocardiograph

PC ECG

ApplicantEdan Instruments, Inc., Shenzhen, Guangdong, CN
DecisionSubstantially Equivalent, Nov 22, 2013
ReceivedJun 20, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K131819

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.