
Smith & Nephew Perry
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PERRY(R) ENCORE CHEMOTHERAPY GLOVE is an FDA 510(k)-cleared medical device (K911633) manufactured by Smith & Nephew Perry. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 8, 1991. Regulation: 8.

Ansell
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SKU VM-1270031