K-number	K131737
Device name	SUPERNOVA C5 MRI SYSTEM
Applicant	Liaoning Kampo Medical System Co., Ltd.
Product code	LNH
Device class	Class II
Decision date	Oct 23, 2014
Decision	Substantially Equivalent
Regulation	892.1000

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Source

View the full FDA submission: accessdata.fda.gov

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SUPERNOVA C5 MRI SYSTEM

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