Etiam S.A.S.U. is one of 289 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Etiam S.A.S.U. - FDA 510(k) Cleared Devices
Recent clearances: ETIAM PACS COMPONENTS
1
Total
1
Cleared
0
Denied
Etiam S.A.S.U. has 1 FDA 510(k) cleared medical devices. Based in Rennes, FR.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Etiam S.A.S.U. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Etiam S.A.S.U.
1 devices