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