K-number	K090785
Device name	MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 865214
Applicant	Invivo Corp.
Product code	MWI
Device class	Class II
Decision date	Dec 15, 2009
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 865214

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