MEDICAL LASER MODEL 5, SURGICAL LASER MODEL 8 & 20 MANUFACTURED BY LUMENIS, INC.

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Request for Information Form	Contact Information
Company Name	LUMENIS, INC.
Address	3959 WEST 1820 SOUTH
City, State, Zip	SALT LAKE CITY, UT 84104
Country	US
FDA Owner/Operator Phone	972-495-99000
FDA Medical Specialty Code	NE - Neurology
FDA Product Code	LLF
FDA Classification Name	LASER, NEUROSURGICAL, ARGON
FDA Device Classification Code	Premarket Approval
FDA Regulation Number	NULL
FDA Common Generic Name	ARGON LASERS
FDA Proprietary Device Name	MEDICAL LASER MODEL 5, SURGICAL LASER MODEL 8 & 20
FDA Owner / Operator Number	9017014
FDA Owner / Operator Name	LUMENIS LTD.
FDA Establishment Registration Number	1720381
FDA Registered Establishment Name	LUMENIS, INC.
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	09-02-92
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A