FDA 510(k) Applications Submitted by Apelem-DMS Group

FDA 510(k) Number Submission Date Device Name Applicant
K160301 02/04/2016 Platinum dRF Imaging System Apelem-DMS Group
K203010 10/01/2020 Platinum dRF Imaging System Apelem-DMS Group
K131766 06/17/2013 PLATINUM DRF IMAGING SYSTEM APELEM-DMS GROUP


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