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FDA 510(k) Applications Submitted by RadiaDyne, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
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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