K-number	K233550
Device name	MOSAIC 3D (Surgical Laser)
Applicant	Lutronic Aesthetic
Product code	ONG
Device class	Class II
Decision date	Jan 2, 2024
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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MOSAIC 3D (Surgical Laser)

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