ClearanceBrief
510(k) K821941 ยท DHR System, Test, Rheumatoid Factor

RHEUMATOID FACTOR REFERENCE PREPARA.

ApplicantArmkel, LLC, Walker MI, US
DecisionSubstantially Equivalent, Aug 27, 1982
ReceivedJun 29, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821941

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.