ClearanceBrief
510(k) K880533 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone

VITEL III CM

ApplicantEquimed Corp., Plymouth MN, US
DecisionSubstantially Equivalent, May 13, 1988
ReceivedFeb 9, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880533

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.