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Steris Corp
Free shipping on orders over $99 · 30-day returns
AMSCO V-PRO is an FDA 510(k)-cleared medical device (K112813) manufactured by Steris Corp. 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 November 30, 2011. Regulation: 8.

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