K-number	K031560
Device name	BAYER RAPIDLAB 1200 SYSTEM
Applicant	Bayer Healthcare, LLC
Product code	CHL
Device class	Class II
Decision date	Dec 17, 2003
Decision	Substantially Equivalent
Regulation	862.1120

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View the full FDA submission: accessdata.fda.gov

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BAYER RAPIDLAB 1200 SYSTEM

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