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Cardiacsense

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2024-05-02
TypeNumberDevice NameCodeDateActions
510(k) K232445 CSF-4 (CSF-4)DPS2024-05-02 View
510(k) K221260 CSF-3DPS2023-01-06 View

Related Clinical Trials

NCT07635602Data Collection Study Using CS BP Pillow SystemCOMPLETEDNCT07749963Data Collection Study Using CS (CardiacSense) BP (Blood Pressure) Watch and Pillow SystemsRECRUITINGNCT06091514Connected Cardiology to Control Cardiac RythmWITHDRAWN
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