K-number	K232085
Device name	DVAS (DVAS-M, DVAS-W)
Applicant	Genoray Co., Ltd.
Product code	EHD
Device class	Class II
Decision date	Dec 8, 2023
Decision	Substantially Equivalent
Regulation	872.1800

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View the full FDA submission: accessdata.fda.gov

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DVAS (DVAS-M, DVAS-W)

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