K-number	K201107
Device name	Opera Lebody (Gold), Opera Lebody (Zafiro)
Applicant	Gtg Wellness Co., Ltd.
Product code	OHS
Device class	Class II
Decision date	Jun 22, 2020
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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Opera Lebody (Gold), Opera Lebody (Zafiro)

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