Medical Device Manufacturer · BE , Leuven

Icometrix - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2016

Total

Cleared

Denied

Icometrix has 2 FDA 510(k) cleared medical devices. Based in Leuven, BE.

Historical record: 2 cleared submissions from 2016 to 2018. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Icometrix Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Icometrix

2 devices

1-2 of 2