FDA 510(k) Applications Submitted by VUCOMP, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K132742 09/03/2013 M-VU BREAST DENSITY VUCOMP, INC.
K060451 02/21/2006 M-VU VIEWER STATION VUCOMP, INC.
K061160 04/26/2006 M-VU CAD STATION VUCOMP, INC.


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