SANDMAN MANUFACTURED BY NELLCOR PURITAN BENNETT (MELVILLE) LTD.

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Request for Information Form	Contact Information
Company Name	NELLCOR PURITAN BENNETT (MELVILLE) LTD.
Address	303 TERRY FOX DR., STE 400
City, State, Zip	KANATA, ONTARIO,
Country	CA
FDA Owner/Operator Phone	925-463-4371
FDA Medical Specialty Code	NE - Neurology
FDA Product Code	GWK
FDA Classification Name	CONDITIONER, SIGNAL, PHYSIOLOGICAL
FDA Device Classification Code	Standards
FDA Regulation Number	882.1845
FDA Common Generic Name	SLEEP EEG SOFTWARE
FDA Proprietary Device Name	SANDMAN
FDA Owner / Operator Number	2936999
FDA Owner / Operator Name	NELLCOR PURITAN BENNETT
FDA Establishment Registration Number	9680138
FDA Registered Establishment Name	NELLCOR PURITAN BENNETT (MELVILLE) LTD.
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	02-12-96
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A

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