BRONCHITRAC DF DUAL RESP/CATHETER

BRONCHITRAC DF DUAL RESP/CATHETER is an FDA 510(k)-cleared medical device (K833633) manufactured by Ackrad Laboratories. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 7, 1983. Regulation: 8.