Medical Device Manufacturer · US , Englewood , CO

Medtronic Hemotec, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1992

Total

Cleared

Denied

Medtronic Hemotec, Inc. has 5 FDA 510(k) cleared medical devices. Based in Englewood, US.

Historical record: 5 cleared submissions from 1992 to 1996. Primary specialty: Hematology.

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

FDA 510(k) Regulatory Record - Medtronic Hemotec, Inc.

5 devices

1-5 of 5