POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE

POWDER FREE CHLORINATED LATEX PATIENT EXAMINATION GLOVE is an FDA 510(k)-cleared medical device (K070760) manufactured by Derma Care Plus Products, LLC. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 6, 2007. Regulation: 8.