HYCARE LATEX EXAMINATION GLOVE, POWDER FREE

HYCARE LATEX EXAMINATION GLOVE, POWDER FREE is an FDA 510(k)-cleared medical device (K020042) manufactured by Hycare Intl. Co., Ltd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 29, 2002. Regulation: 8.