NON-STERILE, POWDERED LATEX EXAMINATION GLOVE

NON-STERILE, POWDERED LATEX EXAMINATION GLOVE is an FDA 510(k)-cleared medical device (K081910) manufactured by Siam Sempermed Corp., Ltd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 16, 2008. Regulation: 8.