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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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