K-number	K052293
Device name	GE 1.5T AND 3.0T SIGNA HDX MR SYSTEM
Applicant	Ge Medical Systems, LLC
Product code	LNH
Device class	Class II
Decision date	Sep 21, 2005
Decision	Substantially Equivalent
Regulation	892.1000

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View the full FDA submission: accessdata.fda.gov

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GE 1.5T AND 3.0T SIGNA HDX MR SYSTEM

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