MindRhythm’s Harmony for Prehospital Large Vessel Occlusion Stroke Identification Submitted for FDA Clearance

MindRhythm Incorporated, a neurodiagnostic company based out of Cupertino, California, today announces it has officially submitted a de novo application to the U.S. Food and Drug Administration (FDA) seeking clearance for its Harmony device designed for prehospital large vessel occlusion (LVO) stroke identification.

We wish UCSF PI Wade Smith, MD, PhD, the best of luck with the FDA.

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