K-number	K150476
Device name	Spectra S1Plus and Spectra S2 Plus
Applicant	Uzinmedicare Co.
Product code	HGX
Device class	Class II
Decision date	Apr 15, 2016
Decision	Substantially Equivalent
Regulation	884.5160

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View the full FDA submission: accessdata.fda.gov

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Spectra S1Plus and Spectra S2 Plus

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