MULTIPLE MANUFACTURED BY BECKMAN COULTER, INC.

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Request for Information Form	Contact Information
Company Name	BECKMAN COULTER, INC.
Address	2470 FARADAY AVE.
City, State, Zip	CARLSBAD, CA 92008
Country	US
FDA Owner/Operator Phone	714-871-4848
FDA Medical Specialty Code	HE - Hematology
FDA Product Code	GKA
FDA Classification Name	ABNORMAL HEMOGLOBIN QUANTITATION
FDA Device Classification Code	Standards
FDA Regulation Number	864.7415
FDA Common Generic Name	PARAGON ACID HEMOGLOBIN
FDA Proprietary Device Name	MULTIPLE
FDA Owner / Operator Number	2050012
FDA Owner / Operator Name	BECKMAN COULTER, INC.
FDA Establishment Registration Number	2050010
FDA Registered Establishment Name	BECKMAN COULTER, INC.
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	09-21-99
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	BIO-RAD LABORATORIES INC., CLINICAL SYSTEMS DIVISI 4000 ALFRED NOBEL DR. HERCULES, CA 94547 US 510-724-7000 / 510-741-6263	BIO-RAD VARIANT NBS SICKLE CELL PROGRAM	SICKLE CELL PROGRAM
2	INTERLAB S.R.L. VIA RINA MONTI N.26 ROME, 00155 IT 390-694-12585 / 570-620-0198	MULTIPLE, INTERLAB ACID HEMOGLOBIN	ACID HEMOGLOBIN TEST SYSTEMS