WARM N WET HMEF W/LUER ADAPTER

WARM N WET HMEF W/LUER ADAPTER is an FDA 510(k)-cleared medical device (K953620) manufactured by Hospitak, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 24, 1995. Regulation: 8.