K-number	K023686
Device name	AURORA MR-GUIDED INTERVENTIONAL SYSTEM
Applicant	Aurora Imaging Technology, Inc.
Product code	LNH
Device class	Class II
Decision date	Jan 29, 2003
Decision	Substantially Equivalent
Regulation	892.1000

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View the full FDA submission: accessdata.fda.gov

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AURORA MR-GUIDED INTERVENTIONAL SYSTEM

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