Medical Device Manufacturer · US , Minneapolis , MN

Aze, Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2006

Total

Cleared

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.

FDA 510(k) Regulatory Record - Aze, Ltd.

3 devices

1-3 of 3