Retia Medical Receives U.S. Food and Drug Administration Clearance for its Innovative Argos Cardiac Output Patient Monitor

VALHALLA, N.Y., Dec. 17, 2018 — Retia Medical, LLC, a medical device company focused on advancing the quality and clinical use of hemodynamic monitoring, today announced that its Argos Cardiac Output (CO) Monitor has received U.S. Food and Drug Administration 510k clearance and is now available for sale in the United States.