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 ID00816870023847
Catalog number10625-300A
AvailabilityPrescription
MRI safetyLabeling does not contain MRI Safety Information
Width7.75 Inch