Meditron AS is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Meditron AS - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Meditron AS has 2 FDA 510(k) cleared medical devices. Based in Chapel Hill, US.
Historical record: 2 cleared submissions from 1999 to 2002. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Meditron AS Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Meditron AS
2 devices