ClearanceBrief
510(k) K071168 ยท DPS Electrocardiograph

THE PORTABLE ANSISCOPE

ApplicantDyansys, Inc., Orinda CA, US
DecisionSubstantially Equivalent, Aug 31, 2007
ReceivedApr 27, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071168

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.