Arcoma AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Arcoma AB - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Arcoma AB
2 devices