ComPAS2 (Computerized Pulmonary Analysis System)

ComPAS2 (Computerized Pulmonary Analysis System) is an FDA 510(k)-cleared medical device (K190568) manufactured by Morgan Scientific, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 5, 2019. Regulation: 8.