Radlogics, Inc. is one of 13048 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Radlogics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AIMI-Triage CXR PTX, ALPHAPOINT IMAGING SOFTWARE
2
Total
2
Cleared
0
Denied
Radlogics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Los Gatos, US.
Historical record: 2 cleared submissions from 2012 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Radlogics, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Hogan Lovells US Lpp.
FDA 510(k) Regulatory Record - Radlogics, Inc.
2 devices