FDA 510(k) Applications for Medical Device Product Code: OAX (Plasmodium Spp. Detection Reagents)

FDA 510(k) Applications for Medical Device Product Code "OAX"
(Plasmodium Spp. Detection Reagents)

FDA 510(k) Number	Applicant	Device Name	Decision Date
DEN070006	INVERNESS MEDICAL PROFESSIONAL DIAGNOSTICS-BINAX	BINAX NOW MALARIA TEST; MODEL 660-000, 660-XXX	06/13/2007