Philips Ultrasound, Inc. - FDA 510(k) Cleared Devices
46
Total
46
Cleared
0
Denied
Philips Ultrasound, Inc. has 46 FDA 510(k) cleared radiology devices. Based in Santa Ana, US.
Last cleared in 2021. Active since 1985.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Philips Ultrasound, Inc.
46 devices
Cleared
Sep 24, 2021
Collaboration Live
Radiology
23d
Cleared
Feb 23, 2021
Lumify Diagnostic Ultrasound System
Radiology
96d
Cleared
Sep 20, 2020
AAA Model
Radiology
195d
Cleared
Sep 15, 2020
Collaboration Live
Radiology
88d
Cleared
Sep 02, 2020
EPIQ Series Diagnostic Ultrasound Systems
Radiology
27d
Cleared
May 14, 2020
PercuNav Image Fusion and Interventional Navigation
Radiology
23d
Cleared
May 01, 2020
EPIQ Diagnostic Ultrasound System Series, Affiniti Diagnostic Ultrasound...
Radiology
14d
Cleared
Mar 06, 2020
EPIQ Diagnostic Ultrasound System
Radiology
29d
Cleared
Nov 09, 2018
EPIQ Diagnostic Ultrasound System, EPIQ 5 Diagnostic Ultrasound System, EPIQ...
Radiology
30d
Cleared
Oct 23, 2018
Xperius Ultrasound System
Radiology
39d
Cleared
Jul 27, 2018
EPIQ , EPIQ 5, EPIQ 7, Affiniti 30, Affiniti 50 and Affiniti 70 Diagnostic...
Radiology
51d
Cleared
Jun 07, 2018
QLAB Advanced Quantification Software
Radiology
24d
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