NON-STERILE E.P. LATEX EXAMINATION GLOVE

NON-STERILE E.P. LATEX EXAMINATION GLOVE is an FDA 510(k)-cleared medical device (K982453) manufactured by Ansell Perry. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 29, 1998. Regulation: 8.