K-number	K230787
Device name	Oscar 15 & Oscar 15i
Applicant	Genoray Co., Ltd.
Product code	OWB
Device class	Class II
Decision date	Jul 20, 2023
Decision	Substantially Equivalent
Regulation	892.1650

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Source

View the full FDA submission: accessdata.fda.gov

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Oscar 15 & Oscar 15i

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