FDA 510(k) Applications Submitted by GENESIS DIGITAL IMAGING, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K130374 02/14/2013 OMNI-VUE 2 SYSTEM GENESIS DIGITAL IMAGING, INC.
K073062 10/30/2007 OMNI-VUE SYSTEM GENESIS DIGITAL IMAGING, INC.


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