BD PROBETEC ET LEGIONELLA PNEUMOPHILA AMPLIFIED DNA ASSAY MANUFACTURED BY BECTON, DICKINSON & CO.

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Request for Information Form	Contact Information
Company Name	BECTON, DICKINSON & CO.
Address	7 LOVETON CIR.
City, State, Zip	SPARKS, MD 21152
Country	US
FDA Owner/Operator Phone	201-847-6800
FDA Medical Specialty Code	MI - Microbiology
FDA Product Code	LQH
FDA Classification Name	DNA-REAGENTS, LEGIONELLA
FDA Device Classification Code	Standards
FDA Regulation Number	866.3300
FDA Common Generic Name	BD PROBETEC ET LEGIONELLA DNA ASSAY
FDA Proprietary Device Name	BD PROBETEC ET LEGIONELLA PNEUMOPHILA AMPLIFIED DNA ASSAY
FDA Owner / Operator Number	9922032
FDA Owner / Operator Name	BECTON, DICKINSON & CO.
FDA Establishment Registration Number	1119779
FDA Registered Establishment Name	BECTON, DICKINSON & CO.
FDA Operation Code(s)	MM - Manufacturer MS - Specification Developer
FDA Listing Date	03-29-03
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	LEGIONELLA ANTISERA " SEIKEN"	LEGIONELLA ANTISERA
2	GEN-PROBE, INC. 10210 GENETIC CENTER DR. SAN DIEGO, CA 92121 US 858-410-8000 / 858-410-8891	GEN-PROBE RAPID DIAGNOSTIC SYSTEM FOR LEGIONELLA	HAEMOPHILUS SPP. SEROLOGICAL REAGENTS
3	MINERVA BIOLABS GMBH KOEPENICKER STRASSE 325 BERLIN, 12555 GM 493-065-762830 / 493-065-762830	ONARLP	LEGIONELLA SPECIES PCR DIAGNOSTIC KIT