Medical Device Manufacturer · US , St. Paul , MN

Tsi, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1985

Total

Cleared

Denied

Tsi, Inc. has 4 FDA 510(k) cleared medical devices. Based in St. Paul, US.

Historical record: 4 cleared submissions from 1985 to 1990. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Tsi, Inc. Filter by specialty or product code using the sidebar.

Tsi, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Tsi, Inc.

4 devices

1-4 of 4