#400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY

#400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY is an FDA 510(k)-cleared medical device (K883593) manufactured by Ecolab, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 29, 1988. Regulation: 8.