Medical Device Manufacturer · BE , Ghent

Epilog - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018

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.

FDA 510(k) Regulatory Record - Epilog

1 devices

1-1 of 1

Cleared Jan 08, 2018

Neurology · 110d