FDAnews
www.fdanews.com/articles/152598-fda-clears-ncontact-8217-s-cardiac-ablation-device

FDA Clears nContact’s Cardiac Ablation Device

January 23, 2013
nContact announced that the FDA has cleared the company’s modifications to its VisiTrax cardiac ablation device, EPi-Sense, now with embedded sensing capability.
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