K-number	K113281
Device name	MRI SYTEMS
Applicant	Shenzhen Anke High-Tech Co., Ltd.
Product code	LNH
Device class	Class II
Decision date	May 17, 2012
Decision	Substantially Equivalent
Regulation	892.1000

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View the full FDA submission: accessdata.fda.gov

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MRI SYTEMS

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