K-number	K091022
Device name	MODIFICATION TO RESERT XL HLD HIGH LEVEL DISINFECTANT
Applicant	STERIS Corporation
Product code	MED
Device class	Class II
Decision date	Apr 12, 2010
Decision	Substantially Equivalent
Regulation	880.6885

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO RESERT XL HLD HIGH LEVEL DISINFECTANT

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