PRE-POWDERED NON-STERILE SYNTHETIC EXAMINATION GLOVE

PRE-POWDERED NON-STERILE SYNTHETIC EXAMINATION GLOVE is an FDA 510(k)-cleared medical device (K982885) manufactured by Shanghai Poseidon Plastic Products Co., Ltd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 3, 1998. Regulation: 8.