ClearanceBrief
510(k) K923578 ยท DHR System, Test, Rheumatoid Factor

LIQUICHEK RHEUMATOID FACTOR CONTROL

ApplicantBio-Rad, Anaheim CA, US
DecisionSubstantially Equivalent, Oct 6, 1992
ReceivedJul 20, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923578

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.