CLK INT'L POWDER FREE LATEX EXAMINATION GLOVE

CLK INT'L POWDER FREE LATEX EXAMINATION GLOVE is an FDA 510(k)-cleared medical device (K974371) manufactured by Clk Intl., Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 20, 1998. Regulation: 8.