LATEX PATIENT EXAMINATION GLOVE, CAT. NO. 1000M POWDERED

LATEX PATIENT EXAMINATION GLOVE, CAT. NO. 1000M POWDERED is an FDA 510(k)-cleared medical device (K982901) manufactured by Vitalcare Group, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 20, 1998. Regulation: 8.