Intromed is one of 22326 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intromed - FDA 510(k) Cleared Devices
Recent clearances: PTFE PEEL AWAY MICROINTRODUCER
1
Total
1
Cleared
0
Denied
Intromed has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Intromed Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Intromed
1 devices