K-number	K231222
Device name	3D OPTICAL COHERENCE TOMOGRAPHY 3D OCT-1(type: Maestro2)
Applicant	Topcon Corporation
Product code	OBO
Device class	Class II
Decision date	Oct 30, 2023
Decision	Substantially Equivalent
Regulation	886.1570

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View the full FDA submission: accessdata.fda.gov

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3D OPTICAL COHERENCE TOMOGRAPHY 3D OCT-1(type: Maestro2)

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