Medical Device Manufacturer · US , Eden Prarie , MN

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

3 submissions · 3 cleared · Since 2009

Total

Cleared

Denied

Hemosphere, Inc. has 3 FDA 510(k) cleared medical devices. Based in Eden Prarie, US.

Historical record: 3 cleared submissions from 2009 to 2012. Primary specialty: Cardiovascular.

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

Hemosphere, 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 - Hemosphere, Inc.

3 devices

1-3 of 3