Resonea, Inc., (“Resonea” or the “Company”) a technology company founded to create a new standard for understanding sleep and breathing and their long-term impact on wellness, performance, and quality of life, announced that they obtained 510(k) clearance from the US Food and Drug Administration (FDA) on July 14, 2019 for their DROWZLE® Sleep Apnea Pre-screening Device.
July 25, 2019
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