Glaxosmithkline Consumer Healthcare is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Glaxosmithkline Consumer Healthcare - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Glaxosmithkline Consumer Healthcare has 3 FDA 510(k) cleared medical devices. Based in Parsippany, US.
Historical record: 3 cleared submissions from 2009 to 2010. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Glaxosmithkline Consumer Healthcare Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Glaxosmithkline Consumer Healthcare
3 devices