ClearanceBrief
510(k) K880283 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone

PACEART PACEMAKER PATIENT TEST SYST/TEL OPT CPTS

ApplicantPaceart, Inc., Wayne NJ, US
DecisionSubstantially Equivalent, Mar 9, 1988
ReceivedJan 22, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880283

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.