Medical Device Manufacturer · SE , Goteborg

Aidera AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009

Total

Cleared

Denied

Aidera AB has 2 FDA 510(k) cleared medical devices. Based in Goteborg, SE.

Historical record: 2 cleared submissions from 2009 to 2010. Primary specialty: General Hospital.

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

Aidera AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Aidera AB

2 devices

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