GUTHRIE PRIME POWDER-FREE CHLORINATED PATIENT EXAMINATION GLOVES

GUTHRIE PRIME POWDER-FREE CHLORINATED PATIENT EXAMINATION GLOVES is an FDA 510(k)-cleared medical device (K000090) 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 February 9, 2000. Regulation: 8.