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FDA Grants NeoVista's Request to Expand CABERNET Trial to 30 Sites in the U.S.
Date:4/17/2008

got approval to apply the CE Mark on its device overseas, giving them ability to distribute and sell its product throughout all EU countries. For more information about the company, the clinical trial or this novel wet AMD therapy, please visit the company's Web site at http://www.neovistainc.com.

Contact: Tony Moses

O: 510.933.7600

C: 510.402.3394

tmoses@neovistainc.com


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SOURCE NeoVista, Inc.
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