LATEX EXAM GLOVE WITH HYPOALLERGENIC LABELING (POWDERED)

LATEX EXAM GLOVE WITH HYPOALLERGENIC LABELING (POWDERED) is an FDA 510(k)-cleared medical device (K960842) manufactured by Crocker Industrial Resources Sdn. Bhd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 18, 1997. Regulation: 8.