
Sgmp Co., Ltd.
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NON-STERILE POWDERED GREEN COLORED POWDERED LATEX PATIENT EXAMINATION GLOVES WITH & WITHOUT SOUR/APPLE/PEPPERMINT SCENTS is an FDA 510(k)-cleared medical device (K030993) manufactured by Sgmp 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 11, 2003. Regulation: 8.

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