FDA 510(k) Applications for Medical Device Product Code: MRS (Test System, Nicotine, Cotinine, Metabolites)

FDA 510(k) Applications for Medical Device Product Code "MRS"
(Test System, Nicotine, Cotinine, Metabolites)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K963733	DYNAGEN, INC.	NICCHECK I	12/13/1996
K030649	MICROGENICS CORP.	DRI COTININE EIA ASSAY	05/22/2003
K021688	NYMOX PHARMACEUTICAL CORPORATION	NICALERT	10/18/2002