NON-STERILE LATEX PROCEDURE GLOVE

NON-STERILE LATEX PROCEDURE GLOVE is an FDA 510(k)-cleared medical device (K900869) manufactured by Sri Johani 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 8, 1990. Regulation: 8.