K-number	K021428
Device name	CLINITEK ATLAS PRO 12 REAGENT PAK SYSTEM
Applicant	Bayer Corp.
Product code	JFY
Device class	Class II
Decision date	Jul 5, 2002
Decision	Substantially Equivalent
Regulation	862.1225

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View the full FDA submission: accessdata.fda.gov

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CLINITEK ATLAS PRO 12 REAGENT PAK SYSTEM

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