ClearanceBrief
510(k) K884800 ยท DPS Electrocardiograph

ACTA GENOS ELECTROCARDIOGRAPH

ApplicantParexel Intl. Corp., Cambridge MS, US
DecisionSubstantially Equivalent, Jun 22, 1989
ReceivedNov 16, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884800

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.