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Company announcement no. 08 2009/10 - The American Health Care Authorities (FDA) have cleared Ambu’s single-use videoscope, Ambu® aScope™



Ambu has been granted the 510K clearance for the Ambu® aScope™ by the American health care authorities. The Ambu® aScope™ consists of two parts, the single-use videoscope and a monitor.

 

With this clearance, the products, which were launched in the European market around New Year 2009, can now be launched, marketed and sold in the American market.

 

Download the annoucement in PDF format.

 

Further information:
Lars Marcher, CEO, phone +45 5136 2490, e-mail: lm@ambu.com

 

 

 - 20-4-2010

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