Philips Consumer Lifestyle is one of 5063 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips Consumer Lifestyle - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Philips Consumer Lifestyle has 2 FDA 510(k) cleared medical devices. Based in Stamford, US.
Historical record: 2 cleared submissions from 2015 to 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Philips Consumer Lifestyle Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Philips Consumer Lifestyle
2 devices