Natus seeks FDA 510(k) clearance for its highly anticipated point-of-care EEG solution ...Middle East

MIDDLETON, Wis., Oct. 10, 2024 /PRNewswire/ -- Natus Medical Incorporated announced it has submitted an FDA 510(k) premarket notification to the U.S. Food and Drug Administration (FDA) for its Natus point-of-care EEG device. Clinicians involved in the system's evaluation expressed high...

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