PRE-POWDER VINYL PATIENT EXAMINATION GLOVES

PRE-POWDER VINYL PATIENT EXAMINATION GLOVES is an FDA 510(k)-cleared medical device (K984461) manufactured by Shanghai Huamao Gloves Co., Ltd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 8, 1999. Regulation: 8.