Epilog is one of 47 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Epilog has 1 FDA 510(k) cleared medical devices. Based in Ghent, BE.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Epilog Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qserve Group, Us, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Epilog
1 devices