K-number	K081600
Device name	STERIS RESERT XL TEST STRIP
Applicant	STERIS Corporation
Product code	JOJ
Device class	Class II
Decision date	Aug 22, 2008
Decision	Substantially Equivalent
Regulation	880.2800

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Source

View the full FDA submission: accessdata.fda.gov

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STERIS RESERT XL TEST STRIP

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