FDA 510(k) Applications Submitted by Deborah Thomas

FDA 510(k) Number Submission Date Device Name Applicant
K230096 01/13/2023 Genius AI Detection 2.0 with CC-MLO Correlation Hologic, Inc.
K201019 04/17/2020 Genius AI Detection Hologic, Inc.
K221449 05/18/2022 Genius AI Detection 2.0 Hologic, Inc.
K111508 06/01/2011 TRIDENT SPECIMEN RADIOGRAPHY SYSTEM, MODEL : RC TRI-00001 HOLOGIC, INC.
K033742 11/28/2003 BOSTON SCIENTIFIC V-18 CONTROL WIRE BOSTON SCIENTIFIC CORP.
K123873 12/17/2012 CONTRAST ENHANCED DIGITAL MAMMOGRAPHY HOLOGIC, INC.


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