ClearanceBrief
510(k) K810306 ยท DHR System, Test, Rheumatoid Factor

RHEUMATOID FACTOR REAGENT TEST KIT

ApplicantBeckman Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 11, 1981
ReceivedFeb 5, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810306

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.