Philips Electronics Nederland B.V. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Philips Electronics Nederland B.V. - FDA 510(k) Cleared Devices
Recent clearances: Philips IntelliSite Pathology Solution
2
Total
2
Cleared
0
Denied
Philips Electronics Nederland B.V. has 2 FDA 510(k) cleared medical devices. Based in Eindhover, NL.
Historical record: 2 cleared submissions from 2017 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Philips Electronics Nederland B.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Philips Electronics Nederland B.V.
2 devices