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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