FDA 510(k) Applications for Medical Device Product Code: MJE (Culture Media, Antifungal, Susceptibility Test)

FDA 510(k) Applications for Medical Device Product Code "MJE"
(Culture Media, Antifungal, Susceptibility Test)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K072827	REMEL, INC.	RPMI 1640 AGAR W/MOPS AND 2% GLUCOSE	11/26/2007