K-number	K130115
Device name	DISCOVERY MR750W 3.0T
Applicant	Ge Medical Systems, LLC
Product code	LNH
Device class	Class II
Decision date	May 23, 2013
Decision	Substantially Equivalent
Regulation	892.1000

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Source

View the full FDA submission: accessdata.fda.gov

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DISCOVERY MR750W 3.0T

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