ADVIA 1650 ALKALINE PHOSPHATASE - AMP ASSAY MANUFACTURED BY SIEMENS MEDICAL SOLUTIONS DIAGNOSTICS

Please Login or Create an Account Now.

This company has been viewed 500 times within the past 60 days.

This product has been viewed: 451 times.

Request for Information Form	Contact Information
Company Name	SIEMENS MEDICAL SOLUTIONS DIAGNOSTICS
Address	511 BENEDICT AVENUE
City, State, Zip	TARRYTOWN, NY 10591
Country	US
FDA Owner/Operator Phone	914-524-2955
FDA Medical Specialty Code	CH - Clinical Chemistry
FDA Product Code	CJK
FDA Classification Name	PHENOLPHTHALEIN PHOSPHATE, ALKALINE PHOSPHATASE OR ISOENZYMES
FDA Device Classification Code	Standards
FDA Regulation Number	862.1050
FDA Common Generic Name	ALKALINE PHOSPHATASE - AMP ASSAY
FDA Proprietary Device Name	ADVIA 1650 ALKALINE PHOSPHATASE - AMP ASSAY
FDA Owner / Operator Number	9096044
FDA Owner / Operator Name	SIEMENS MEDICAL SOLUTIONS DIAGNOSTICS
FDA Establishment Registration Number	2432235
FDA Registered Establishment Name	SIEMENS MEDICAL SOLUTIONS DIAGNOSTICS
FDA Operation Code(s)	MM - Manufacturer MS - Specification Developer
FDA Listing Date	04-30-02
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A