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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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