K-number	K053462
Device name	3160 MRI PATIENT MONITORING SYSTEM
Applicant	Invivo Corporation
Product code	MWI
Device class	Class II
Decision date	Jan 18, 2006
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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3160 MRI PATIENT MONITORING SYSTEM

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