K-number	K010534
Device name	CROSS-CHECKS DUAL, MODEL CI 125
Applicant	Steritec Products, Inc.
Product code	JOJ
Device class	Class II
Decision date	Aug 6, 2001
Decision	Substantially Equivalent
Regulation	880.2800

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View the full FDA submission: accessdata.fda.gov

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CROSS-CHECKS DUAL, MODEL CI 125

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