Mitsubishi Kagaku Iatron is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mitsubishi Kagaku Iatron - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Mitsubishi Kagaku Iatron has 4 FDA 510(k) cleared medical devices. Based in Seattle, US.
Historical record: 4 cleared submissions from 2008 to 2009. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Mitsubishi Kagaku Iatron Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mitsubishi Kagaku Iatron
4 devices