Medical Device Manufacturer · US , Andover , MA

Philips Ultrasound - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2004

Total

Cleared

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.

Philips Ultrasound is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Philips Ultrasound

5 devices

1-5 of 5