SAS RUBBER PRODUCTS CO./LATEX EXAMINATION GLOVES

SAS RUBBER PRODUCTS CO./LATEX EXAMINATION GLOVES is an FDA 510(k)-cleared medical device (K911939) manufactured by Overseas Import & Export Dist.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 14, 1991. Regulation: 8.