510(k) K172754

V-PRO maX 2 Low Temperature Sterilization System by STERIS Corporation — Product Code MLR

K172754 is an FDA 510(k) premarket notification submitted by STERIS Corporation for the device "V-PRO maX 2 Low Temperature Sterilization System". The FDA issued a decision of Substantially Equivalent on February 9, 2018. The device falls under product code MLR (Sterilizer, Chemical), a Class II device regulated under 21 CFR 880.6860. STERIS Corporation has at least 10 other 510(k) clearances on record.