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# Zoll Brain Injury Dashboard Cleared
- URL: https://www.fdaweb.com/zoll-brain-injury-dashboard-cleared/
- Published: 2021-07-21T12:00:00.000Z
- Updated: 2026-09-14T17:07:09.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5149759

FDA has cleared a Zoll Medical 510(k) for its TBI Dashboard feature on its Propaq M monitor and Propaq MD monitor/defibrillator. The dashboard provides clinical decision support for managing patients with traumatic brain injury, and was previously available on Propaq devices sold in international markets. The device is designed to assist treatment of military-related traumatic brain injuries. It displays numeric and graphical trend data on hypotension, hypoxia, and hyperventilation. “Providing continuously updated vital-signs data at a glance allows medical personnel to make treatment decisions before a patient’s status becomes critical,” the company says. The dashboard also includes a breath-by-breath countdown timer to help care providers maintain proper ventilation rates and prevent hyperventilation, it says.