OX-SOX, MODEL C, D, E,

OX-SOX, MODEL C, D, E, is an FDA 510(k)-cleared medical device (K062300) manufactured by Pattient Safety Innovations, Llp. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 26, 2006. Regulation: 8.