LATEX EXAMINATION GLOVES BUBBLE GUM FLAVOURED PRE-POWDERED

LATEX EXAMINATION GLOVES BUBBLE GUM FLAVOURED PRE-POWDERED is an FDA 510(k)-cleared medical device (K981600) manufactured by Young Innovations, LLC Dba Plak Smacker. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 1, 1998. Regulation: 8.