K-number	K230024
Device name	HI-EMT MAGSHAPE
Applicant	Beijing Sano Laser S&T Development Co.,Ltd
Product code	NGX
Device class	Class II
Decision date	Sep 6, 2023
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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HI-EMT MAGSHAPE

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