K-number	K050672
Device name	ERCHONIA EVRL LASER
Applicant	Erchonia Medical, Inc.
Product code	GEX
Device class	Class II
Decision date	May 2, 2005
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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ERCHONIA EVRL LASER

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