UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUIT

UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUIT is an FDA 510(k)-cleared medical device (K953787) manufactured by Unicor, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 18, 1995. Regulation: 8.