MULTIPLE-FLEX MANUFACTURED BY GUIDANT CORPORATION, CARDIAC SURGERY

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Request for Information Form	Contact Information
Company Name	GUIDANT CORPORATION, CARDIAC SURGERY
Address	170 BAYTECH DRIVE
City, State, Zip	SAN JOSE, CA 95134
Country	US
FDA Owner/Operator Phone	317-971-2000
FDA Medical Specialty Code	SU - General Plastic Surgery
FDA Product Code	NEY
FDA Classification Name	SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES
FDA Device Classification Code	Standards
FDA Regulation Number	878.4400
FDA Common Generic Name	ABLATION SYSTEM
FDA Proprietary Device Name	MULTIPLE-FLEX
FDA Owner / Operator Number	9019904
FDA Owner / Operator Name	GUIDANT CORPORATION
FDA Establishment Registration Number	3006262933
FDA Registered Establishment Name	GUIDANT CORPORATION, CARDIAC SURGERY
FDA Operation Code(s)	MS - Specification Developer
FDA Listing Date	04-12-07
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 companies may manufacture a similar device.

	Company Name / Address / Phone	Proprietary Device Name	Common Generic Device Name
1	GUIDANT CORPORATION, CARDIAC SURGERY 3200 LAKESIDE DR. SANTA CLARA, CA 95054 US 317-971-2000 / 408-845-2060	MICROWAVE ABLATION SYSTEM AND ACCESSORIES	MICROWAVE GENERATOR, FLEX 10, FLEX 4
2	GUIDANT PUERTO RICO B.V. #12, RD. #698 DORADO, PR 00646 US 651-582-4000 / 651-582-5656	MULTIPLE-FLEX	ABLATION SYSTEM
3	MICROSULIS MEDICAL LTD. PARKLANDS BUSINESS PARK DENMEAD HAMPSHIRE, PO7 6XP UK 44-23-92240011 / 442-392-242535	MICROSULIS TISSULE ABLATION SYSTEM	ELECTROSURGICAL CUTTING AND COAGULATION DEVICE AND ACCESS