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www.fdanews.com/articles/108685-misonix-receives-fda-approval-of-second-soft-tissue-ablation-system

Misonix Receives FDA Approval of Second Soft Tissue Ablation System

July 18, 2008
Misonix, a developer of minimally invasive ultrasonic medical device technology, which in Europe is used for the ablation of cancer and worldwide for other acute health conditions, has received 510(k) clearance from the U.S. Food and Drug Administration to market its Sonatherm 600i High Intensity Focused Ultrasound Soft Tissue Ablation System in the United States. …
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