K-number	K200516
Device name	OCT-Camera ID 21101A3
Applicant	Optomedical Technologies GmbH
Product code	OBO
Device class	Class II
Decision date	Sep 2, 2020
Decision	Substantially Equivalent
Regulation	886.1570

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Source

View the full FDA submission: accessdata.fda.gov

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OCT-Camera ID 21101A3

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