Imi is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Imi - FDA 510(k) Cleared Devices
1
Total
0
Cleared
0
Denied
Imi has 0 FDA 510(k) cleared medical devices. Based in Rockville, US.
Historical record: 0 cleared submissions from 2002 to 2002. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Imi Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Imi
1 devices