POWDERFREE NITRILE NEOPRENE EXAMINATION GLOVES (PULPLE)

POWDERFREE NITRILE NEOPRENE EXAMINATION GLOVES (PULPLE) is an FDA 510(k)-cleared medical device (K012786) manufactured by Shamrock Manufacturing Company. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 30, 2001. Regulation: 8.