NEOTECH MUCUS TRAP W/CATHETER

NEOTECH MUCUS TRAP W/CATHETER is an FDA 510(k)-cleared medical device (K890425) manufactured by Neotech Products, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 18, 1989. Regulation: 8.