ClearanceBrief
510(k) K882686 ยท GGT Assay, Erythropoietin

ERYTHROPOIETIN ENZYME IMMUNOASSAY

ApplicantAmgen, Inc., Thousand Oaks CA, US
DecisionSubstantially Equivalent, Dec 20, 1988
ReceivedJun 30, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882686

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.