GUTHRIE POWDERFREE LATEX EXAMINATION GLOVES

GUTHRIE POWDERFREE LATEX EXAMINATION GLOVES is an FDA 510(k)-cleared medical device (K954967) manufactured by Guthrie Medicare Products (Melaka) Sdn Bhd. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 14, 1996. Regulation: 8.