Philips Healthcare (Suzhou) Co., Ltd. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Philips Healthcare (Suzhou) Co., Ltd. has 17 FDA 510(k) cleared radiology devices. Based in Suzhou Jiangsu, CN.
Latest FDA clearance: Mar 2026. Active since 2014.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Philips Medical Systems Technologies , Ltd. as regulatory consultant.
17 devices
Cleared
Mar 23, 2026
CT Rembra RT
Radiology
186d
Cleared
Mar 20, 2026
Smart Fit TorsoCardiac 1.5T
Radiology
31d
Cleared
Nov 18, 2024
CT Collaboration Live
Radiology
104d
Cleared
May 03, 2024
CT 5300
Radiology
260d
Cleared
Feb 05, 2024
Smart Fit Knee 3.0T
Radiology
88d
Cleared
Sep 01, 2023
Smart Fit TorsoCardiac 1.5T and Smart Fit Shoulder 1.5T
Radiology
56d
Cleared
Dec 22, 2022
Philips CT 3500
Radiology
55d
Cleared
Apr 27, 2022
Philips Incisive CT
Radiology
266d
Cleared
Dec 01, 2021
dS TorsoCardiac 1.5T, dS MSK S 1.5T, dS MSK M 1.5T
Radiology
84d
Cleared
Nov 22, 2021
Philips Incisive CT on Trailer
Radiology
217d
Cleared
Jun 17, 2021
Precise Position
Radiology
199d
Cleared
Jul 09, 2020
DuraDiagnost
Radiology
23d