Philips Ultrasound - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Philips Ultrasound has 5 FDA 510(k) cleared medical devices. Based in Andover, US.
Latest FDA clearance: May 2025. Active since 2004. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Philips Ultrasound Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Philips Ultrasound
5 devices
Cleared
May 15, 2025
Lumify Diagnostic Ultrasound System
Radiology
265d
Cleared
May 08, 2025
Lumify Diagnostic Ultrasound System
Radiology
245d
Cleared
Oct 26, 2023
Lumify Diagnostic Ultrasound System
Radiology
70d
Cleared
May 04, 2023
Lumify Diagnostic Ultrasound System
Radiology
139d
Cleared
Feb 17, 2004
QLAB QUANTIFICATION SOFTWARE
Radiology
15d