K-number	K201663
Device name	AcuPulse W CO2 Laser Systems, Delivery Devices and Accessories
Applicant	Lumenis, Ltd.
Product code	GEX
Device class	Class II
Decision date	Jul 16, 2020
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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AcuPulse W CO2 Laser Systems, Delivery Devices and Accessories

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