Getinge receives US FDA 510(k) clearance for three products, expanding the Servo ventilator platform.
Getinge receives US FDA 510(k) clearance for three products, expanding the Servo ventilator platform. 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 software upgrades, Getinge also received clearance for the new Servo-u MR ventilator for the MRI room. Uppdaterad 2021-04-22 Publicerad 2021-04-22 “The COVID-19 pandemic and the heightened awareness of respiratory health have driven the need for personalized ventilation solutions for critic...
Source: realtid.se