OMNI F.T. LATEX EXAMINATION GLOVE, POWDERED

OMNI F.T. LATEX EXAMINATION GLOVE, POWDERED is an FDA 510(k)-cleared medical device (K973134) manufactured by Omnigrace , Ltd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 5, 1997. Regulation: 8.