SENSICARE POWDER FREE MEDICAL GLOVE

SENSICARE POWDER FREE MEDICAL GLOVE is an FDA 510(k)-cleared medical device (K925244) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 18, 1993. Regulation: 8.