ClearanceBrief
510(k) K812972 ยท DHR System, Test, Rheumatoid Factor

RA LATEX TEST

ApplicantOxoid U.S.A., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 6, 1981
ReceivedOct 23, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812972

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.