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

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

FDA 510(k) Number	Applicant	Device Name	Decision Date
K220991	Cytovale Inc.	IntelliSep test	12/20/2022
K250513	Cytovale, Inc.	IntelliSep Test (CV-ICG-048)	03/21/2025

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