K-number	K161509
Device name	3D OCT-1 Maestro
Applicant	Topcon Corporation
Product code	OBO
Device class	Class II
Decision date	Jul 28, 2016
Decision	Substantially Equivalent
Regulation	886.1570

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Source

View the full FDA submission: accessdata.fda.gov

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3D OCT-1 Maestro

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