ClearanceBrief
510(k) K012407 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone

PACEART TX3 CARDIAC EVENT RECORDER

ApplicantPaceart, Inc., Hasbrouck Heights NJ, US
DecisionSubstantially Equivalent, Aug 14, 2001
ReceivedJul 30, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K012407

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.