K-number	K220926
Device name	Spectra Wearable
Applicant	Uzinmedicare Co., Ltd.
Product code	HGX
Device class	Class II
Decision date	Dec 12, 2022
Decision	Substantially Equivalent
Regulation	884.5160

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Source

View the full FDA submission: accessdata.fda.gov

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Spectra Wearable

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