Biosense Webster is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biosense Webster - FDA 510(k) Cleared Devices
Recent clearances: TruDi Navigation System
3
Total
3
Cleared
0
Denied
Biosense Webster has 3 FDA 510(k) cleared medical devices. Based in Diamond Bar, US.
Historical record: 3 cleared submissions from 2014 to 2020. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Biosense Webster Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acclarent, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Biosense Webster
3 devices