K-number	K233933
Device name	CIRRUS HD-OCT Model 6000
Applicant	Carl Zeiss Meditec, Inc.
Product code	OBO
Device class	Class II
Decision date	May 17, 2024
Decision	Substantially Equivalent
Regulation	886.1570

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Source

View the full FDA submission: accessdata.fda.gov

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CIRRUS HD-OCT Model 6000

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CIRRUS HD-OCT Model 6000