Ekeroth Quality AB is one of 102 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Ekeroth Quality AB - FDA 510(k) Cleared Devices
Recent clearances: DYNAWELL OR DYNAWELL
1
Total
1
Cleared
0
Denied
Ekeroth Quality AB has 1 FDA 510(k) cleared medical devices. Based in Stockholm, SE.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ekeroth Quality AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ekeroth Quality AB
1 devices