K-number	K102330
Device name	AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM
Applicant	STERIS Corporation
Product code	MLR
Device class	Class II
Decision date	Aug 12, 2011
Decision	Substantially Equivalent
Regulation	880.6860

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View the full FDA submission: accessdata.fda.gov

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AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM

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