STERIS Corporation
VERIFY ASSERT STEAM Process Challenge Device
SKU K162945UPC OWP
In Stock
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IIFDA 510(k) Cleared (K162945)
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Free shipping on orders over $99 · 30-day returns
STERIS Corporation
Free shipping on orders over $99 · 30-day returns
VERIFY ASSERT STEAM Process Challenge Device is an FDA 510(k)-cleared medical device (K162945) 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 April 27, 2017. Regulation: 8.
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