K-number	K942861
Device name	MEDVISION ENVIROMENT/MEDVISION 2.0
Applicant	Evergreen Technologies, Inc.
Product code	LMD
Device class	Class I
Decision date	Dec 7, 1994
Decision	Substantially Equivalent
Regulation	892.2020

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View the full FDA submission: accessdata.fda.gov

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MEDVISION ENVIROMENT/MEDVISION 2.0

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