Aurora Technology Development, LLC is one of 18577 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aurora Technology Development, LLC - FDA 510(k) Cleared Devices
Recent clearances: Adaptivo
1
Total
1
Cleared
0
Denied
Aurora Technology Development, LLC has 1 FDA 510(k) cleared medical devices. Based in Madison, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Aurora Technology Development, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Speed TO Market, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Aurora Technology Development, LLC
1 devices