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Movano secures clearance for pulse ox 

December 2, 2024HME News Staff

PLEASANTON, Calif. – Movano Health has announced U.S. Food and Drug Administration 510(k) clearance for the pulse oximeter in its EvieMED Ring. The company says the clearance enables it to pursue multi-billion-dollar business opportunities for health monitoring solutions needed for applications such as clinical trials, post-clinical trial management and remote patient monitoring for both health care providers and payers. "We launched the Evie Ring in the consumer wearable market, but our...

EvieMED Ring, FDA clearance, Movano Health, Pulse oximeters, Remote Patient Monitoring

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