K-number	K222400
Device name	Coresculpt & Magsculpt
Applicant	K1Med Co., Ltd.
Product code	NGX
Device class	Class II
Decision date	Feb 27, 2024
Decision	Substantially Equivalent
Regulation	890.5850

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Source

View the full FDA submission: accessdata.fda.gov

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Coresculpt & Magsculpt

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