Airsonett AB is one of 5186 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Airsonett AB - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Airsonett AB has 1 FDA 510(k) cleared medical devices. Based in Fridley, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Airsonett AB Filter by specialty or product code using the sidebar.
Airsonett AB — FDA 510(k) Products and Clearance History
1 devices