ClearanceBrief
510(k) K832054 ยท DCK C-Reactive Protein, Antigen, Antiserum, And Control

FIAX CRP TEST KIT

ApplicantIntl. Diagnostic Technology, Mchenry IL, US
DecisionSubstantially Equivalent, Aug 26, 1983
ReceivedJun 27, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832054

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.