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

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

FDA 510(k) Number	Applicant	Device Name	Decision Date
K243566	Cardiosense, Inc.	CardioTagÖ	07/22/2025
K160656	CorSens Medical Ltd.	CorSens	11/21/2016
K081603	HEARTFORCE MEDICAL, INC.	DIGITAL BALLISTOCARDIOGRAPH, MODEL DGB 300	07/24/2009