K-number	K211761
Device name	UltraLase Flexible CO2 Laser Waveguide
Applicant	W & R Investments, LLC Dba Laser Engineering
Product code	GEX
Device class	Class II
Decision date	Jul 30, 2021
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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UltraLase Flexible CO2 Laser Waveguide

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