
Ansell Perry
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ENCORE MARK IV POWDER FREE POLYMER COATED LATEX SURGICAL GLOVE WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LE) is an FDA 510(k)-cleared medical device (K983489) 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 December 13, 1998. Regulation: 8.