The Maquet SERVO-i ventilator battery module has been recalled due to the battery having a shorter run time than expected, according to the American Society of Anesthesiologists. The FDA assigned a ...
Getinge receives US FDA 510(k) clearance for three products, expanding the Servo ventilator platform
GÖTEBORG, Sweden, April 22, 2021 /PRNewswire/ -- Today, Getinge announces clearance from the US FDA of several new software options for the Servo-u and Servo-n ventilators. In addition to the latest ...
Central sleep apnea is associated with poor prognosis and death in patients with heart failure. Adaptive servo-ventilation is a therapy that uses a noninvasive ventilator to treat central sleep apnea ...
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