K-number	K153739
Device name	MRI Patient Monitor TeslaDUO
Applicant	Mipm Mammendorfer Institut Fur Physik Und Medizin
Product code	MWI
Device class	Class II
Decision date	Jun 28, 2016
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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MRI Patient Monitor TeslaDUO

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