Philips India Limited is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Philips India Limited - FDA 510(k) Cleared Devices
Recent clearances: StentBoost Mobile
2
Total
2
Cleared
0
Denied
Philips India Limited has 2 FDA 510(k) cleared medical devices. Based in Pune, IN.
Last cleared in 2021. Active since 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Philips India Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Philips India Limited
2 devices