DUNFORD SURGEON'S STERILE GLOVES

DUNFORD SURGEON'S STERILE GLOVES is an FDA 510(k)-cleared medical device (K880480) manufactured by Phillippine Radiant C/O U.S. Polymer Industries. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 16, 1988. Regulation: 8.