Medical Device Manufacturer · BE , Leuven

Icometrix - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2016

Recent clearances: icobrain, icobrain

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.

Icometrix is one of 42 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Icometrix

2 devices

1-2 of 2