FDA 510(k) Applications Submitted by GORDON SHU

FDA 510(k) Number Submission Date Device Name Applicant
K180015 01/02/2018 Philips Incisive CT Philips Healthcare (Suzhou) Co., Ltd.
K141381 05/27/2014 DURADIAGNOST PHILIPS HEALTHCARE (SUZHOU) CO., LTD.
K173507 11/13/2017 Prodiva 1.5T CX and Prodiva 1.5T CS R5.4 Philips Healthcare (Suzhou) Co., Ltd.


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