FDA 510(k) Applications for Medical Device Product Code: JSX (Kit, Identification, Neisseria Gonorrhoeae)

FDA 510(k) Applications for Medical Device Product Code "JSX"
(Kit, Identification, Neisseria Gonorrhoeae)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K960759	MEDTEX LABORATORIES, INC.	GONOPOX TEST KIT	09/18/1996