K-number	K233065
Device name	V-PRO maX 2 Low Temperature Sterilization System
Applicant	Steris
Product code	MLR
Device class	Class II
Decision date	Oct 20, 2023
Decision	Substantially Equivalent
Regulation	880.6860

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Source

View the full FDA submission: accessdata.fda.gov

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V-PRO maX 2 Low Temperature Sterilization System

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