K-number	K110434
Device name	TRIXEL CO2 LASER
Applicant	BEIJING SYNTECH LASER CO., LTD.
Product code	GEX
Device class	Class II
Decision date	Apr 19, 2011
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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TRIXEL CO2 LASER

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