Interventional Innovations Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Interventional Innovations Corp. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Interventional Innovations Corp. has 2 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 2 cleared submissions from 1996 to 1997. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Interventional Innovations Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Interventional Innovations Corp.
2 devices