Movano Health announced today that it received FDA 510(k) clearance for the pulse oximeter in its EvieMED Ring.

(RTTNews) - Movano Inc. (MOVE), Monday announced that the pulse oximeter in the company's EvieMED Ring has received 510 (k) clearance from the U.S. Food and Drug Administration. The company explained ...

Movano Health plans to market the Evie Ring to organizations that run clinical trials and healthcare companies that are helping patients manage chronic diseases.

Movano Health has announced U.S. Food and Drug Administration 510(k) clearance for the pulse oximeter in its EvieMED Ring ...

Health announced U.S. Food and Drug Administration, FDA, 510(k) clearance for the pulse oximeter in its EvieMED Ring. The ...

Securing FDA 510(k) clearance for the EvieMED Ring and pursuing initial business-to-business (B2B) commercial agreements across the healthcare sector. Advancing cuffless blood pressure and ...

The EvieMED Ring is a wearable device designed to not only provide medical device functionality through its pulse oximetry feature, but also offer numerous wellness metrics related to sleep ...

Nov. 4, 2024 /PRNewswire/ -- Movano Health (NASDAQ: MOVE) announced today that it has submitted a complete response package to the FDA as part of the final phase of the Company's 510(k) application ...

PLEASANTON, Calif. - Movano Health (NASDAQ:MOVE) announced today that it is preparing to submit responses to the FDA's latest inquiries regarding its EvieMED Ring, a device under the 510(k ...

"We are confident we can effectively address the follow up questions that the Agency has submitted, and we look forward to completing the final review of the EvieMED Ring." The EvieMED Ring is a ...

PLEASANTON, Calif. - Movano Health (NASDAQ:MOVE) announced today that it is preparing to submit responses to the FDA's latest inquiries regarding its EvieMED Ring, a device under the 510(k) review ...