AMERICAN PHARMASEAL HUMIDAIR CONDENSER

AMERICAN PHARMASEAL HUMIDAIR CONDENSER is an FDA 510(k)-cleared medical device (K854012) manufactured by American Pharmaseal Div. Ahsc. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 2, 1985. Regulation: 8.