Ambient Clinical Analytics is one of 19064 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ambient Clinical Analytics - FDA 510(k) Cleared Devices
Recent clearances: AWARE
1
Total
1
Cleared
0
Denied
Ambient Clinical Analytics has 1 FDA 510(k) cleared medical devices. Based in Rochester, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ambient Clinical Analytics 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 - Ambient Clinical Analytics
1 devices