Lifebridge Medizintechnik AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lifebridge Medizintechnik AG - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Lifebridge Medizintechnik AG has 3 FDA 510(k) cleared medical devices. Based in Bryn Mawr, US.
Historical record: 3 cleared submissions from 2009 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Lifebridge Medizintechnik AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lifebridge Medizintechnik AG
3 devices