LATEX EXAMINATION GLOVES, MODIFICATION-NONPOWDERED

LATEX EXAMINATION GLOVES, MODIFICATION-NONPOWDERED is an FDA 510(k)-cleared medical device (K915052) manufactured by Supertex Glove Intl. Corp.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 8, 1993. Regulation: 8.