ClearanceBrief
510(k) K791948 ยท GQH Antigen, Cf (Including Cf Control), Cytomegalovirus

FIAX TEST KIT FOR ANTI-CYTOMEGALORIRUS

ApplicantIntl. Diagnostic Technology, Mchenry IL, US
DecisionSubstantially Equivalent, Nov 16, 1979
ReceivedOct 1, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791948

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.