FDA 510(k) Applications for Medical Device Product Code: PEO ()

FDA 510(k) Applications for Medical Device Product Code "PEO"

FDA 510(k) Number	Applicant	Device Name	Decision Date
K182690	GenMark Diagnostics, Incorporated	ePlex Blood Culture Identification Panel Fungal Pathogen (BCID-FP) Panel	12/21/2018
K240627	Luminex Corporation	LIAISON PLEX Yeast Blood Culture Assay	06/04/2024