Euromi S.A is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Euromi S.A - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Euromi S.A has 2 FDA 510(k) cleared medical devices. Based in Huntington, US.
Historical record: 2 cleared submissions from 2001 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Euromi S.A Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Euromi S.A
2 devices