K-number	K160433
Device name	V-PRO® 1 Plus and V-PRO® maX Low Temperature
Applicant	STERIS Corporation
Product code	MLR
Device class	Class II
Decision date	Jul 6, 2016
Decision	Substantially Equivalent
Regulation	880.6860

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View the full FDA submission: accessdata.fda.gov

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V-PRO® 1 Plus and V-PRO® maX Low Temperature

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