QUIDEL QUICKVUE HELICOBACTER PYLORI TEST MANUFACTURED BY QUIDEL CORP.

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Request for Information Form	Contact Information
Company Name	QUIDEL CORP.
Address	10165 MCKELLAR CT.
City, State, Zip	SAN DIEGO, CA 92121
Country	US
FDA Owner/Operator Phone	858-552-1100
FDA Medical Specialty Code	MI - Microbiology
FDA Product Code	LQP
FDA Classification Name	CAMPYLOBACTER SPP.
FDA Device Classification Code	General Controls
FDA Regulation Number	866.3110
FDA Common Generic Name	HELICOBACTER PYLORI TEST SYSTEM
FDA Proprietary Device Name	QUIDEL QUICKVUE HELICOBACTER PYLORI TEST
FDA Owner / Operator Number	2024674
FDA Owner / Operator Name	QUIDEL CORP.
FDA Establishment Registration Number	2024674
FDA Registered Establishment Name	QUIDEL CORP.
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	12-22-92
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	DENKA SEIKEN CO., LTD (NIIGATA FACILITY) 1-2-2, MINAMI HONCHO GOSEN-SHI, NIIGATA, 959-1695 JA 81-3-36699421 / 81-250-420812	MULTIPLE	VARIOUS ANTISERA OF CAMPYLOBACTER
2	OXOID, LTD. WADE RD. BASINGSTOKE, HAMPSHIRE, RG24 8PW UK 603-929-2650 / 412-490-8425	MULTIPLE	CAMPYLOBACTER
3	PANBIO, INC. 9075 GUILFORD RD. COLUMBIA, MD 21046 US 410-381-8550 231 / 410-381-8550 231	CAMPY (JCL)	CAMPY (JCL)
4	REMEL EUROPE LTD REMEL HOUSE, CLIPPER BLVD. WEST CROSSWAYS DARTFORD, KENT, DA2 6PT UK 412-490-8425 / 412-490-8425	CAMPYLOBACTER	MICROPLATE ASSAY