SENSORMEDICS MODEL 922 SPIROMETER

SENSORMEDICS MODEL 922 SPIROMETER is an FDA 510(k)-cleared medical device (K920246) manufactured by Sensor Medics Corp.. 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 7, 1992. Regulation: 8.