FDA 510(k) Applications Submitted by 3DISC AMERICAS

FDA 510(k) Number Submission Date Device Name Applicant
K131442 05/20/2013 FIRECR DENTALIMAGING SYSTEM 3DISC AMERICAS
K102619 09/13/2010 COMPUTED RADDIOGRAPHY SCANNER 3DISC AMERICAS
K133106 09/30/2013 COMPUTED RADIOGRAPHY SCANNER 3DISC AMERICAS
K133120 09/30/2013 COMPUTED RADIOGRAPHY SCANNER 3DISC AMERICAS
K151687 06/23/2015 QuantorView 3DISC AMERICAS


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