Cefar Medical AB is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cefar Medical AB - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Cefar Medical AB has 2 FDA 510(k) cleared medical devices. Based in Minneapolis,, US.
Historical record: 2 cleared submissions from 2002 to 2003. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Cefar Medical AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cefar Medical AB
2 devices