GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE

GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE is an FDA 510(k)-cleared medical device (K993793) 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 January 11, 2000. Regulation: 8.