Device typeAdrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA): A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of the adrenocorticotropic hormone (ACTH) in a clinical specimen, using an enzyme immunoassay (EIA) method.
FDA categoryRadioimmunoassay, Acth
Device ID14560189212517
Single useYes
MRI safetyLabeling does not contain MRI Safety Information