Arcoma AB is one of 127 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Arcoma AB - FDA 510(k) Cleared Devices
Recent clearances: 0180 INTUITION, 0072 PRECISION, INTUITION, MODEL 0170
2
Total
2
Cleared
0
Denied
Arcoma AB has 2 FDA 510(k) cleared medical devices. Based in Vaxjo, SE.
Historical record: 2 cleared submissions from 2008 to 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Arcoma AB Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Intertek Testing Services and Acroma AB.
FDA 510(k) Regulatory Record - Arcoma AB
2 devices