ENDOPATH MANUFACTURED BY ETHICON ENDO-SURGERY, LLC

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Request for Information Form	Contact Information
Company Name	ETHICON ENDO-SURGERY, LLC
Address	475 CALLE C
City, State, Zip	GUAYNABO, PR 00969
Country	US
FDA Owner/Operator Phone	787-653-4608
FDA Medical Specialty Code	GU - Gastroenterology/Urology
FDA Product Code	FDP
FDA Classification Name	APPARATUS, PNEUMOPERITONEUM, AUTOMATIC
FDA Device Classification Code	Standards
FDA Regulation Number	876.1500
FDA Common Generic Name	INSUFFLATION NEEDLE
FDA Proprietary Device Name	ENDOPATH
FDA Owner / Operator Number	9071406
FDA Owner / Operator Name	ETHICON ENDO-SURGERY, LLC
FDA Establishment Registration Number	3005075853
FDA Registered Establishment Name	ETHICON ENDO-SURGERY, LLC
FDA Operation Code(s)	MS - Specification Developer
FDA Listing Date	10-09-05
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	ENTRACARE, LLC 11315 STRANG LINE RD. LENEXA, KS 66215 US 913-451-2234 / 913-451-2234 15	MULTIPLE	ENTERAL PUMP AND GRAVITY FEEDING SETS, NON-STERILE
2	ETHICON ENDO-SURGERY, INC. 4545 CREEK RD. CINCINNATI, OH 45242 US 513-337-7000 / 513-337-3134	ENDOPATH	INSUFFLATION NEEDLE