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Vitrolife: Application for Market Approval of STEEN Solution™ in the USA Has Been Submitted to the FDA


7/10/2012 10:08:39 AM

GÖTEBORG, Sweden--(BUSINESS WIRE)--Regulatory News: Vitrolife (STO:VITR) has submitted an application to the American Food and Drug Administration (FDA) regarding market approval of STEEN Solution™, a product used for cleansing and evaluation of lungs outside the body (ex vivo) before transplantation.

Read at BioSpace.com


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