POWDERED VINYL PATIENT GLOVE

POWDERED VINYL PATIENT GLOVE is an FDA 510(k)-cleared medical device (K070046) manufactured by Shijiazhuang Lianhe Shunda Plastic Products Co., L. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 6, 2007. Regulation: 8.