K-number	K242441
Device name	Revian Lyte (10011)
Applicant	Revian, Inc.
Product code	OAP
Device class	Class II
Decision date	Sep 13, 2024
Decision	Substantially Equivalent
Regulation	890.5500

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Source

View the full FDA submission: accessdata.fda.gov

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Revian Lyte (10011)

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