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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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