ClearanceBrief
510(k) K020806 ยท LOJ Kit, Test,Alpha-Fetoprotein For Testicular Cancer

ACS:180 & ADVIA CENTAUR AFP IMMUNOASSAY

ApplicantBayer Corp., Medfield MA, US
DecisionSubstantially Equivalent, Mar 27, 2002
ReceivedMar 12, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K020806

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.