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invendo medical Files 510(K) Notice With FDA for Clearance of the Computer-Assisted Colonoscopy System
Date:3/8/2010

served during the study. Lesions were detected in 41% of the subjects.

The C20™ colonoscopy system has already received CE mark in Europe.

"Our initial commercial focus will be on the United States," said Berthold Hackl, CEO of invendo medical, "Therefore the submission for 510(k) clearance of our new colonoscopy system marks a major milestone in our company's history. We will give the further process with the U.S. Food and Drug Administration our full attention."

About invendo medical - www.invendo-medical.com

Based in New York, U.S.A. and Kissing (near Munich), Germany, invendo medical is a leading developer of disposable endoscopy products in the field of gastroenterology that are hygienically safe an
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