TRIACTIV SYSTEM MANUFACTURED BY KENSEY NASH CORP.

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Request for Information Form	Contact Information
Company Name	KENSEY NASH CORP.
Address	735 PENNSYLVANIA DRIVE
City, State, Zip	EXTON, PA 19341
Country	US
FDA Owner/Operator Phone	484-713-2100
FDA Medical Specialty Code	CV - Cardiovascular
FDA Product Code	NFA
FDA Classification Name	DEVICE, CORONARY SAPHENOUS VEIN BYPASS GRAFT, TEMPORARY, FOR EMBOLIZATION PROTECTION
FDA Device Classification Code	Standards
FDA Regulation Number	870.1250
FDA Common Generic Name	EMBOLIC PROTECTION DEVICE
FDA Proprietary Device Name	TRIACTIV SYSTEM
FDA Owner / Operator Number	9020253
FDA Owner / Operator Name	KENSEY NASH CORP.
FDA Establishment Registration Number	2530154
FDA Registered Establishment Name	KENSEY NASH CORP.
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	03-28-05
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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