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

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


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