Getinge receives 510(k) clearance from US FDA for the Servo-air® mechanical ventilator
Getinge has received 510(k) clearance from the US Food & Drug Administration (FDA) for the company’s Servo-air® mechanical ventilator, which is part of the Servo family that supports intensive care ventilation ever since the first model was introduced in 1971.[Mekanisk ventilator ]
"We are happy to be able to help clinicians in their endeavor to save lives by adding an additional ventilator to our product offering in the US market,” says Elin Frostehav, Vice President Critical Care at Getinge. “This is also an important step for our ventilation business in other parts of the world where
