RESPIRATORY AIRWAY TUBE MONITOR (RATM)

RESPIRATORY AIRWAY TUBE MONITOR (RATM) is an FDA 510(k)-cleared medical device (K883158) manufactured by Vascucare, 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 March 5, 1989. Regulation: 8.