Lazarus 3D, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lazarus 3D, Inc. has 1 FDA 510(k) cleared medical devices. Based in Corvallis, US.
Last cleared in 2021. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Lazarus 3D, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Obelix Consulting as regulatory consultant.
1 devices