LOPRO SILICONISED LOW PROTEIN POWDERFREE LATEX EXAMINATION GLOVES

LOPRO SILICONISED LOW PROTEIN POWDERFREE LATEX EXAMINATION GLOVES is an FDA 510(k)-cleared medical device (K982114) manufactured by M/S Midland Latex Products , Ltd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 20, 1999. Regulation: 8.