K-number	K203142
Device name	Veuron-Brain-pAb
Applicant	Heuron Co., Ltd.
Product code	LLZ
Device class	Class II
Decision date	Jan 15, 2021
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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Veuron-Brain-pAb

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