May 19, 2020

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    Press releases

    June 18, 2020

    FDA and Health Canada Approve Thermedical’s Degassed Saline to Help Reduce
    Risk of Stroke
    FDA and Health Canada Approve Thermedical’s Degassed Saline to Help Reduce
    Risk of Stroke

    May 18, 2020

    Thermedical Announces FDA Breakthrough Device Designation
    Thermedical Announces FDA Breakthrough Device Designation

    May 8, 2020

    Thermedical Announces SERF VT Study Presented as Part of HRS 2020 Science Late-Breaking Clinical Trial Sessions May 2020
    Thermedical Announces SERF VT Study Presented as Part of HRS 2020 Science Late-Breaking Clinical Trial Sessions May 2020

    July 31, 2018

    Thermedical Announces FDA IDE Clearance
    Thermedical Announces FDA IDE Clearance

    March 20, 2018

    Thermedical Announces Series A Financing Round
    Thermedical Announces Series A Financing Round

    October 31, 2012

    Thermedical Announces FDA 510(k) Clearance
    Thermedical Announces FDA 510(k) Clearance

    October 27, 2006

    NIH Awards Thermedical $3.6M to Test for Prevention of Sudden Cardiac Death
    NIH Awards Thermedical $3.6M to Test for Prevention of Sudden Cardiac Death

    The Thermedical® Ablation System is 510(k) cleared for the coagulation and ablation of soft tissue during percutaneous, laparoscopic and intraoperative surgical procedures.  Use of the Thermedical Ablation System for any specific soft tissue indication has not been evaluated or approved by the US FDA.

    Use of the Thermedical Ablation System for the treatment of VT is investigational and is not approved for use or sale in any market.

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