K-number	K232464
Device name	VereSee Optical Veres Needle System
Applicant	Freyja Healthcare, LLC
Product code	HIF
Device class	Class II
Decision date	May 2, 2024
Decision	Substantially Equivalent
Regulation	884.1730

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Source

View the full FDA submission: accessdata.fda.gov

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VereSee Optical Veres Needle System

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