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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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