CARESCAPE CO2 Microstream parameter

CARESCAPE CO2 Microstream parameter is an FDA 510(k)-cleared medical device (K213518) manufactured by Covidien, LLC. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 11, 2022. Regulation: 8.