POWDERED LATEX EXAM GLOVES WITH PROTEIN LABELING (200UG/G OR LESS)

POWDERED LATEX EXAM GLOVES WITH PROTEIN LABELING (200UG/G OR LESS) is an FDA 510(k)-cleared medical device (K022530) 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 August 25, 2002. Regulation: 8.