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Sunmax Enterprise Shanghai Co. , Ltd.
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SUNMAX ENTERPRISE SHANGHAI CO. POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVE TESTED WITH CHEMOTHERAPY DRUGS is an FDA 510(k)-cleared medical device (K090336) manufactured by Sunmax Enterprise Shanghai Co. , Ltd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 30, 2009. Regulation: 8.

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