FDA 510(k) Applications Submitted by VIDISTAR, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K152822 09/28/2015 VidiStar HeartView VIDISTAR, LLC
K083910 12/30/2008 VIDISTAR PACS & DICOM VIEWER SOFTWARE SERVER SOFTWARE SYSTEM, HEART VIEW, STANDALONE VIEWER VIDISTAR, LLC


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