ClearanceBrief
510(k) K871041 ยท DHR System, Test, Rheumatoid Factor

RF MICROASSAY

ApplicantDiamedix Corp., Miami FL, US
DecisionSubstantially Equivalent, Mar 31, 1987
ReceivedMar 17, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K871041

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.