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

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

FDA 510(k) Number	Applicant	Device Name	Decision Date
K191194	Carl Zeiss Meditec, Inc	CLARUS	06/25/2019
K181444	Carl Zeiss Meditec, Inc.	CLARUS	01/10/2019

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