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

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

FDA 510(k) Number	Applicant	Device Name	Decision Date
K181412	bioMerieux, Inc.	VITEK MS	12/21/2018
K212461	bioMerieux, Inc.	VITEK MS PRIME	03/15/2022
DEN170081	Bruker Daltonik GmbH	MALDI Biotyper CA System	04/20/2018

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