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STERIS Corporation
Free shipping on orders over $99 · 30-day returns
VERIFY CHEMICAL MONITORING STRIP FOR RESERT SOULTIONS (RESERT XL TEST STRIP VERSION 2) is an FDA 510(k)-cleared medical device (K102296) manufactured by STERIS Corporation. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 8, 2011. Regulation: 8.

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