Aze, Ltd. is one of 18984 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aze, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: AZE PHOENIX SOFTWARE, AZE VIRTUALPLACE-MR FLOW ANALYSIS SOFTWARE, AZE VIRTUALPLACE
3
Total
3
Cleared
0
Denied
Aze, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 3 cleared submissions from 2006 to 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Aze, Ltd. 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 - Aze, Ltd.
3 devices