K-number	K061258
Device name	TRABECTOME HIGH FREQUENCY GENERATOR/LP
Applicant	Neomedix Corp.
Product code	GEI
Device class	Class II
Decision date	May 18, 2006
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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TRABECTOME HIGH FREQUENCY GENERATOR/LP

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