Ig Technology, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ig Technology, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Sheffield, GB.
Last cleared in 2023. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ig Technology, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
1 devices