POWDERFREE NITRILE PATIENT EXMINATION GLOVE

POWDERFREE NITRILE PATIENT EXMINATION GLOVE is an FDA 510(k)-cleared medical device (K003985) 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 8, 2001. Regulation: 8.