News | March 21, 2007

MAQUET Gains FDA Clearance to Upgrade Ventilator System

March 22, 2007 – MAQUET Critical Care recently announced that they have received FDA clearance for an upgrade of its SERVO-i Ventilator System for conditional use in the magnetic resonance (MR) environment.

The SERVO-i ventilator is intended for treatment and monitoring of all patients who require mechanical ventilation. The new MR option is capable of providing critically ill patients with advanced ventilatory care using the same machine wherever they are in the hospital, the ICU, the MR examination room and during transport to and from the MR room.

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