Dicom Grid 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 Dba Ambra Health - FDA 510(k) Cleared Devices
Recent clearances: Ambra PACS
1
Total
1
Cleared
0
Denied
Dicom Grid Dba Ambra Health has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Last cleared in 2023. Active since 2023. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dicom Grid Dba Ambra Health Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dicom Grid Dba Ambra Health
1 devices