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Article: Siemens Receives FDA Approval for the VERSANT 440 Molecular System.
- Article from:
- PR Newswire
- Article date:
- February 18, 2008
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Copyright informationCOPYRIGHT 2008 PR Newswire Association LLC. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan. All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)
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Siemens Offers Next Generation Molecular Viral Load Testing to the U.S. Market
DEERFIELD, Ill., Feb. 18 /PRNewswire/ -- Siemens Healthcare (http://www.siemens.com/diagnostics) announced today that its VERSANT(TM) 440 Molecular System has been approved for marketing by the U.S. Food and Drug Administration (FDA) for use with the VERSANT HCV RNA 3.0 assay for management of HCV-infected patients undergoing antiviral therapy. The VERSANT 440 Molecular System represents the next generation in automated viral load testing, providing laboratories with greater throughput and less hands-on time, maximizing productivity to meet the evolving needs of the clinical laboratory.
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