K-number	K050399
Device name	MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 3160
Applicant	Invivo Research, Inc.
Product code	MWI
Device class	Class II
Decision date	Aug 26, 2005
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 3160

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