ClearanceBrief
510(k) K002310 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone

CARDIOBEEPER CB12/12, MODEL CB12/12

ApplicantMeridian Medical Technologies , Ltd., Belfast, IE
DecisionSubstantially Equivalent, Oct 25, 2000
ReceivedJul 31, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002310

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.