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Pyng Medical Corp's FASTResponder Receives CE Mark In Europe And Cleared By FDA For Marketing In United States


Thursday, 27 Jun 2013 07:04pm EDT 

Pyng Medical Corp announced that FASTResponder, its Intraosseus Infusion device, has received the CE Mark in Europe and has been cleared by the United States Food and Drug Administration (FDA) for marketing in the United States. The FASTResponder product has received initial positive input from medical professionals regarding it being easy to learn and easy to use. Such feedback indicates the possibility of opening up usage of Pyng Intraosseus Infusion products to a wider range of applications and markets. 

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