MULTIPLE, INTERLAB ACID HEMOGLOBIN MANUFACTURED BY INTERLAB S.R.L.

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Request for Information Form	Contact Information
Company Name	INTERLAB S.R.L.
Address	VIA RINA MONTI N.26
City, State, Zip	ROME,
Country	IT
FDA Owner/Operator Phone	390-694-12585
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	ACID HEMOGLOBIN TEST SYSTEMS
FDA Proprietary Device Name	MULTIPLE, INTERLAB ACID HEMOGLOBIN
FDA Owner / Operator Number	9056968
FDA Owner / Operator Name	INTERLAB S.R.L.
FDA Establishment Registration Number	3003961883
FDA Registered Establishment Name	INTERLAB S.R.L.
FDA Operation Code(s)	MS - Specification Developer RR - Repackager/Relabeller
FDA Listing Date	02-06-04
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	BECKMAN COULTER, INC. 2470 FARADAY AVE. CARLSBAD, CA 92008 US 714-871-4848 / 714-993-5321 8383	MULTIPLE	PARAGON ACID HEMOGLOBIN
2	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