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FDA 510(k) Applications Submitted by GIOTTO USA, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K062039
07/19/2006
BIOPSY DIGIT-AM
GIOTTO USA, LLC
K113607
12/06/2011
BIOPSY DIGIT S BIOPSY SL
GIOTTO USA, LLC
K111434
05/23/2011
GIOTTO IMAGE 3D, GIOTTO IMAGE 3D-L
GIOTTO USA, LLC
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