Getinge receives 510(k) clearance from US FDA for software upgrade in Servo-u® and Servo-n® ventilator platform
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 ventilator platform. This software release includes the addition of Servo Compass® and High Flow therapy as well as additional advancements for ventilation therapy support.“This is an important milestone for Getinge’s ventilation business in the US”, says Jens Viebke, President Acute Care Therapies at Getinge. “With the innovative options for Servo Compass and High Flow therapy we can meet the demand from our US customers to support the