Medical Device Manufacturer · US , Santa Barbara , CA

Interventional Therapeutics Corp. - FDA 510(k) Cleared Devices

28 submissions · 27 cleared · Since 1987
28
Total
27
Cleared
0
Denied

Interventional Therapeutics Corp. has 27 FDA 510(k) cleared medical devices. Based in Santa Barbara, US.

Historical record: 27 cleared submissions from 1987 to 1996. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Interventional Therapeutics Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Interventional Therapeutics Corp.
28 devices
1-12 of 28
Filters