KAHN-TACT U.S.A., EFF LARYNGOSCOPE

KAHN-TACT U.S.A., EFF LARYNGOSCOPE is an FDA 510(k)-cleared medical device (K872480) manufactured by Effner and Spreine Co.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 9, 1987. Regulation: 8.