SLIM EVOLUTION (PREVIOUSLY MULTIPULSE) MANUFACTURED BY LASERING S.R.L.

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Request for Information Form	Contact Information
Company Name	LASERING S.R.L.
Address	VIA STAFFETTE PARTIGIANE,54
City, State, Zip	MODENA,
Country	IT
FDA Owner/Operator Phone	390-594-50999
FDA Medical Specialty Code	NE - Neurology
FDA Product Code	GXE
FDA Classification Name	LEUKOTOME
FDA Device Classification Code	General Controls
FDA Regulation Number	882.4600
FDA Common Generic Name	CO2 SURGICAL LASER
FDA Proprietary Device Name	SLIM EVOLUTION (PREVIOUSLY MULTIPULSE)
FDA Owner / Operator Number	9042050
FDA Owner / Operator Name	LASERING S.R.L.
FDA Establishment Registration Number	3004710757
FDA Registered Establishment Name	LASERING S.R.L.
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	07-31-06
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A

Our records indicate that the following medical device companyies may manufacture a similar device.

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1	SP MEDICAL A/S MOLLEVEJ 1 KARISE, DK-4653 DA 45-56-766000 / 45-56-766000	MULTIPLE	DISPOSABLE MONOPOLAR NEEDLE ELECTRODES