K-number	K153283
Device name	VivoSight Dx Topical OCT System
Applicant	Michelson Diagnostics, Ltd.
Product code	NQQ
Device class	Class II
Decision date	Aug 11, 2016
Decision	Substantially Equivalent
Regulation	892.1560

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Source

View the full FDA submission: accessdata.fda.gov

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VivoSight Dx Topical OCT System

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