V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System

V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System is an FDA 510(k)-cleared medical device (K222093) manufactured by Steris. 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 September 8, 2022. Regulation: 8.