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Home » FDA Clears Philips’ Remote Monitoring Defibrillator Platform
FDA Clears Philips’ Remote Monitoring Defibrillator Platform
Philips has earned 510(k) clearance from the FDA for its Tempus ALS platform, a remote patient monitoring and defibrillator system.
The system consists of a portable monitor that tracks vital signs and a defibrillator that connect wirelessly to share collected data and images to a web-based software platform.
The device and software platform “will help front line responders provide emergency care, diagnosis and treatment,” including defibrillation therapy and data management, the company said.
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