BREAKING NEWS:
US Medical Innovations Receives FDA 510(k) Clearance for the Canady Plasma Smart XL-1000 Generator
Clinical Trial using Canady Helios™ Cold Plasma Therapy for Solid Tumors
FDA# G190165
Treatment of Triple-Negative Breast Cancer Cells with the Canady Cold Plasma Conversion System: Preliminary Results
X. Cheng, W. Rowe, L. Ly, A. Shashurin, T. Zhuang, S. Wigh, G. Basadonna, B. Trink, M. Keidar and J. Canady
Plasma 2018, 1, 218–228; doi:10.3390/plasma1010019
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US Medical Innovations Receives FDA 510(k) Clearance for the Canady Plasma Smart XL-1000 Generator
https://www.businesswire.com/news/home/20191125005726/en/Medical-Innovations-Receives-FDA-510-Clearance-Canady
https://www.businesswire.com/news/home/20191125005726/en/Medical-Innovations-Receives-FDA-510-Clearance-Canady
US Medical Innovations Receives FDA 510(k) Clearance for the Canady Plasma Smart XL-1000 Generator
US Medical Innovations has received FDA 510(k) clearance for the Canady Plasma® Smart XL-1000™ Electrosurgical Generator
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Dr. Jerome Canady presenting at the 3rd Semi-Annual Medical Device Human Factors & Usability Conference in Alexandria, Virginia #AnalogToSmartTechnology #CanadyHybridPlasmaTechnology #ColdPlasma #Robotics
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US Medical Innovations, LLC (USMI), based out of Takoma Park, MD, is a privately-held FDA registered life science and biomedical device company. USMI is dedicated to expanding the boundaries of plasma medicine by pioneering new technologies for the development of state-of-the-art medical devices that advance patient outcomes and improve human lives.