FDA 510(k) Applications Submitted by JOHN K. ISHAM

FDA 510(k) Number Submission Date Device Name Applicant
K182395 09/04/2018 OARtrac System RadialDyne, LLC
K150719 03/19/2015 OARtrac System with Skin Sensors RadiaDyne, LLC
K162954 10/24/2016 OARtrac System with Patient Specific Reusable Universal PSD Sensors RADIADYNE, LLC


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