dailyfreeman.com

Getinge receives US FDA 510(k) clearance for three products, expanding the Servo ventilator platform

GOTEBORG, 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 ...
Business Insider

Getinge Receives 510(k) Clearance From US FDA for Software Upgrade in Servo-u® and Servo-n® Ventilator Platform

GETINGE, Sweden, April 10, 2019 /PRNewswire/ -- Getinge is today announcing clearance from the US Food & Drug Administration (FDA) for a new software version for the Servo-u® and Servo-n® mechanical ...
Becker's ASC

Maquet’s SERVO-i Ventilator Battery Module Given Class 1 Recall

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 ...
The New England Journal of Medicine

Adaptive Servo-Ventilation for Central Sleep Apnea in Systolic Heart Failure

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 ...