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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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