ClearanceBrief
510(k) K791282 ยท DGQ Whole Blood Plasma, Antigen, Antiserum, Control

ANTI-HUMAN SERUM

ApplicantDiagnostica, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 17, 1979
ReceivedJul 10, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791282

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.