K-number	K121738
Device name	MYVISIONTRACK(TM)
Applicant	Vital Art and Science Incorporated
Product code	HOQ
Device class	Class I
Decision date	Feb 22, 2013
Decision	Substantially Equivalent
Regulation	886.1330

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Source

View the full FDA submission: accessdata.fda.gov

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MYVISIONTRACK(TM)

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