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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
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3DISC AMERICAS
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