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Ansell Perry
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ENCORE MICROPTIC POWDER FREE LATEX SURGICAL GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS) is an FDA 510(k)-cleared medical device (K000295) manufactured by Ansell Perry. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 15, 2000. Regulation: 8.