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

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

FDA 510(k) Number	Applicant	Device Name	Decision Date
K223905	Avicena, LLC	Vivio« LVEDP System	10/06/2023
K222463	Ultromics Limited	EchoGo Heart Failure	11/23/2022
K240013	Ultromics Limited	EchoGo Heart Failure (2.0)	09/23/2024

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