K-number	K083665
Device name	VERIFY SCBI 275F 3-10
Applicant	STERIS Corporation
Product code	FRC
Device class	Class II
Decision date	Sep 1, 2009
Decision	Substantially Equivalent
Regulation	880.2800

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View the full FDA submission: accessdata.fda.gov

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VERIFY SCBI 275F 3-10

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