K-number	K130290
Device name	MODIFICATION TO INTEL-GE CARE IINOVATIONS GUIDE
Applicant	Intel-Ge Care Innovations, LLC
Product code	DRG
Device class	Class II
Decision date	Jun 4, 2013
Decision	Substantially Equivalent
Regulation	870.2910

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO INTEL-GE CARE IINOVATIONS GUIDE

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