Medos Medizintechnik AG is one of 19639 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medos Medizintechnik AG - FDA 510(k) Cleared Devices
Recent clearances: MEDOS HILITE INFANT OXYGENATOR, MEDOS HILITE OXYGENATOR, MEDOS HILITE 7000 & 7000 LT OXYGENATOR
3
Total
3
Cleared
0
Denied
Medos Medizintechnik AG has 3 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.
Historical record: 3 cleared submissions from 2014 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medos Medizintechnik AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medos Medizintechnik AG
3 devices