Echopixel, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Echopixel, Inc. - FDA 510(k) Cleared Devices
Recent clearances: True 3D Viewer, True 3D Viewer Software
4
Total
4
Cleared
0
Denied
Echopixel, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 4 cleared submissions from 2015 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Echopixel, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Sheila Pickering Consulting Group.
FDA 510(k) Regulatory Record - Echopixel, Inc.
4 devices