OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE

OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE is an FDA 510(k)-cleared medical device (K980419) manufactured by Omnigrace (Thailand) , Ltd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 12, 1998. Regulation: 8.