BSD Medical files 510(k) submission for premarket clearance of Phase II MTX-180
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BSD Medical files 510(k) submission for premarket clearance of Phase II MTX-180
BSD Medical Corporation today announced that the Company has filed a 510(k) submission with the U.S. Food and Drug Administration for premarket clearance of the Company's Phase II MicroThermX® Microwave Ablation System for ablation of soft tissue.
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Most Recently Shared on March 22, 2010 at 4:59 pm By:
Oncology News: BSD Medical files 510(k) submission for premarket clearance of Phase II MTX-180: BSD Medical Corpor... http://bit.ly/cZy8WB
BSD receives FDA review questions for Phase II MTX-180 Microwave Ablation System 510(k) submission
news-medical.net — “BSD Medical Corporation today announced that it has received review questions from the U.S. Food and Drug Administration (FDA) regarding the 510(k) submission the Company filed for premarket clearance of the Company's Phase II MicroThermX® Microwave Ablation System (MTX-180) for ablation of soft tissue.” View full resource at news-medical.net
Most Recently Shared on July 12, 2010 at 5:46 pm By:
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Oncology News: BSD receives FDA review questions for Phase II MTX-180 Microwave Ablation System 510(k) submission:... http://bit.ly/asnM3a
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