Philips DS North America, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips DS North America, LLC - FDA 510(k) Cleared Devices
Recent clearances: UroNav 4
1
Total
1
Cleared
0
Denied
Philips DS North America, LLC has 1 FDA 510(k) cleared medical devices. Based in Gainesville, US.
Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Philips DS North America, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Philips DS North America, LLC
1 devices