STERIS Corporation
V-PRO® 1 Plus and V-PRO® maX Low Temperature
SKU K160433UPC MLR
In Stock
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IIFDA 510(k) Cleared (K160433)
1
Free shipping on orders over $99 · 30-day returns
STERIS Corporation
Free shipping on orders over $99 · 30-day returns
V-PRO® 1 Plus and V-PRO® maX Low Temperature is an FDA 510(k)-cleared medical device (K160433) 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 July 5, 2016. Regulation: 8.
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