K-number	K120979
Device name	CAREFUSION NICOLET EDX
Applicant	Carefusion 209, Inc.
Product code	GWF
Device class	Class II
Decision date	Apr 25, 2012
Decision	Substantially Equivalent
Regulation	882.1870

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View the full FDA submission: accessdata.fda.gov

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CAREFUSION NICOLET EDX

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