K-number	K223322
Device name	Argus Cognitive ReVISION Software
Applicant	Argus Cognitive, Inc.
Product code	LLZ
Device class	Class II
Decision date	Jul 24, 2023
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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Argus Cognitive ReVISION Software

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