Medical Device Manufacturer · CH , Lausanne

Aimago SA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2012

Total

Cleared

Denied

Aimago SA has 2 FDA 510(k) cleared medical devices. Based in Lausanne, CH.

Historical record: 2 cleared submissions from 2012 to 2013. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Aimago SA Filter by specialty or product code using the sidebar.

Aimago SA is one of 89 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.

Aimago SA — FDA 510(k) Products and Clearance History

2 devices

1-2 of 2