Home » Dade Behring Submits 510(k) for Dimension Vista 1500 Analyzer
Dade Behring Submits 510(k) for Dimension Vista 1500 Analyzer
Dade Behring announced its 510(k) submission to the FDA for a Class I device classification for the Dimension Vista 1500 System, the company's first integrated chemistry/immunochemistry system targeted at high-volume clinical laboratory customers. The Dimension Vista System is targeted for commercialization in the second half of 2006.
Business Wire (http://home.businesswire.com/portal/site/google/index.jsp?ndmViewId=news_view&newsId=20050427006061&newsLang=en)
KEYWORDS FDAnews Device Daily Bulletin
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