ClearanceBrief
510(k) K823934 ยท DYC Vectorcardiograph

CARIEL F12

ApplicantOdam, France, FR
DecisionSubstantially Equivalent, Dec 16, 1983
ReceivedDec 29, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823934

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.