ClearanceBrief
510(k) K092010 ยท DPS Electrocardiograph

PC ECG, MODEL SE-1010

ApplicantEdan Instruments, Inc., Yonkers NY, US
DecisionSubstantially Equivalent, Oct 22, 2009
ReceivedJul 6, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092010

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.