LATEX PATIENT EXAMINATION GLOVE POWDER FREE (HYPOALLERGENIC)

LATEX PATIENT EXAMINATION GLOVE POWDER FREE (HYPOALLERGENIC) is an FDA 510(k)-cleared medical device (K946257) manufactured by Siam Sempermed Corp., Ltd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 7, 1995. Regulation: 8.