VYGON DOUBLE LUMEN UMBILICAL CATHETER MANUFACTURED BY VYGON CORP.

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Request for Information Form	Contact Information
Company Name	VYGON CORP.
Address	2495 GENERAL ARMISTEAD AVE
City, State, Zip	NORRISTOWN, PA 19403
Country	US
FDA Owner/Operator Phone	610-539-9300
FDA Medical Specialty Code	HO - General Hospital
FDA Product Code	FOS
FDA Classification Name	CATHETER, UMBILICAL ARTERY
FDA Device Classification Code	Standards
FDA Regulation Number	880.5200
FDA Common Generic Name	PEDIATRIC DOUBLE LUMEN UMBILICAL CATHETER
FDA Proprietary Device Name	VYGON DOUBLE LUMEN UMBILICAL CATHETER
FDA Owner / Operator Number	2245270
FDA Owner / Operator Name	VYGON CORP.
FDA Establishment Registration Number	2245270
FDA Registered Establishment Name	VYGON CORP.
FDA Operation Code(s)	RR - Repackager/Relabeller
FDA Listing Date	11-10-98
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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