K-number	K061624
Device name	VITREA, VERSION 3.9
Applicant	Vital Images, Inc.
Product code	LLZ
Device class	Class II
Decision date	Jun 27, 2006
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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VITREA, VERSION 3.9

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