K-number	K063159
Device name	STERILOX LIQUID CHEMICAL STERILANT SYSTEM
Applicant	Puricore, Inc.
Product code	MED
Device class	Class II
Decision date	Apr 2, 2007
Decision	Substantially Equivalent
Regulation	880.6885

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View the full FDA submission: accessdata.fda.gov

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STERILOX LIQUID CHEMICAL STERILANT SYSTEM

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