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FDA Reclassifies ECP Devices for Refractory Angina as Class II
Date:1/6/2014

roducts and their pricing; medical insurance reimbursement policies; unexpected manufacturing or supplier problems; unforeseen difficulties and delays in the conduct of clinical trials and other product development programs; the actions of regulatory authorities and third-party payers in the United States and overseas; uncertainties about the acceptance of a novel therapeutic modality by the medical community; continuation of the GEHC agreement; and the risk factors reported from time to time in the Company's SEC reports.  The Company undertakes no obligation to update forward-looking statements as a result of future events or developments.

Investor Contacts: 
Todd Fromer / Garth Russell
KCSA Strategic Communications
212-896-1215 / 212-896-1250 
tfromer@kcsa.com / grussell@kcsa.com  

Media Contact:
Samantha Wolf
KCSA Strategic Communications
212-896-1220 
swolf@kcsa.com


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SOURCE Vasomedical, Inc.
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