Intelligence Artificielle Applications is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intelligence Artificielle Applications - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Intelligence Artificielle Applications has 1 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Intelligence Artificielle Applications Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intelligence Artificielle Applications
1 devices