FDA 510(k) Applications for Medical Device Product Code: DJP (Radioimmunoassay, Amphetamine)

FDA 510(k) Applications for Medical Device Product Code "DJP"
(Radioimmunoassay, Amphetamine)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K960526	DIAGNOSTIC REAGENTS, INC.	PRIMIDONE EIA TEST	03/18/1996