Acotec Scientific Holdings Ltd receives US FDA 510k clearance for Endovenous Radiofrequency Ablation System
Reuters
Oct 09
Acotec Scientific Holdings Ltd receives US FDA 510k clearance for Endovenous Radiofrequency Ablation System
Acotec Scientific Holdings Ltd. has announced that its Endovenous Radiofrequency Ablation System has received 510(k) clearance from the U.S. Food and Drug Administration (FDA). The system, which includes the Cedar™ Endovenous Radiofrequency Catheters and the Endovenous Radiofrequency Generator, is designed for the treatment of lower extremity varicose veins caused by superficial venous reflux. Acotec has also entered into a distribution agreement with a member of the BSC Group for the product's distribution in the United States, with commercialization to begin when appropriate.
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