FTA- ABS SORBENT MANUFACTURED BY BAUSCH & LOMB, INC.

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Request for Information Form	Contact Information
Company Name	BAUSCH & LOMB, INC.
Address	499 SOVEREIGN CT.
City, State, Zip	MANCHESTER, MO 63011
Country	US
FDA Owner/Operator Phone	585-338-6000
FDA Medical Specialty Code	MI - Microbiology
FDA Product Code	GMW
FDA Classification Name	TEST, SORBENT, FTA-ABS
FDA Device Classification Code	Standards
FDA Regulation Number	866.3830
FDA Common Generic Name	FTA- ABS SORBENT
FDA Proprietary Device Name	FTA- ABS SORBENT
FDA Owner / Operator Number	9913003
FDA Owner / Operator Name	BAUSCH & LOMB, INC.
FDA Establishment Registration Number	1932180
FDA Registered Establishment Name	BAUSCH & LOMB, INC.
FDA Operation Code(s)	MM - Manufacturer MR - Remanufacturer RR - Repackager/Relabeller
FDA Listing Date	01-12-93
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	CENTERS FOR DISEASE CONTROL AND PREVENTION 1600 CLIFTON RD., N.E. ATLANTA, GA 30333 US / 404-639-3042	SORBENT STANDARDIZING SERUM (FTA-ABS). HUMAN	SORBENT STANDARDIZING SERUM (FTA-ABS). HUMAN
2	LEE LABORATORIES, INC. 1475 ATHENS HWY. GRAYSON, GA 30017 US 201-847-6800 / 410-316-4000 4099		SORBENT FOR FTA-ABS TEST