Dicom Grid Inc Dba Ambra Health is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dicom Grid Inc Dba Ambra Health - FDA 510(k) Cleared Devices
Recent clearances: Ambra ProViewer
1
Total
1
Cleared
0
Denied
Dicom Grid Inc Dba Ambra Health has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dicom Grid Inc Dba Ambra Health Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Accelerated Device Approval Services as regulatory consultant.
FDA 510(k) Regulatory Record - Dicom Grid Inc Dba Ambra Health
1 devices