CIRCULITE® RECEIVES CONDITIONAL IDE APPROVAL FOR SYNERGY® CIRCULATORY SUPPORT SYSTEM FEASIBILITY TRIAL

MINIMALLY-INVASIVE SYSTEM DESIGNED TO REVERSE HEART FAILURE FILLS TREATMENT GAP FOR AMBULATORY CHRONIC HEART FAILURE PATIENTS

SADDLE BROOK, NJ (March 5, 2013) CircuLite®, Inc. today announced that it has received conditional approval from the United States Food and Drug Administration (FDA) of an Investigational Device Exemption (IDE) for its lead product, the SYNERGY® Circulatory Support System, a minimally-invasive device designed to reverse the symptoms of heart failure in ambulatory chronic heart failure patients.

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Categories: Life Sciences Industry Network

Author:NJ Tech Council

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