K-number	K230342
Device name	Phototherapy System (OL-PDT950)
Applicant	Shanghai Omni Laser Skinology Co., Ltd.
Product code	GEX
Device class	Class II
Decision date	Aug 16, 2023
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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Phototherapy System (OL-PDT950)

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