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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, X-Ray, Tomography, Computed
510(k) Number K180015
Device Name Philips Incisive CT
Applicant
Philips Healthcare (Suzhou) Co., Ltd.
No.258, ZhongYuan Road, Suzhou Industrial Park
Suzhou,  CN 215024
Applicant Contact Gordon Shu
Correspondent
Philips Healthcare (Suzhou) Co., Ltd.
No.258, ZhongYuan Road, Suzhou Industrial Park
Suzhou,  CN 215024
Correspondent Contact Shiguang An
Regulation Number892.1750
Classification Product Code
JAK  
Date Received01/02/2018
Decision Date 03/20/2018
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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