Medical Device Manufacturer · US , West Lafayette , IN

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

5 submissions · 5 cleared · Since 1994

Total

Cleared

Denied

Hemocleanse, Inc. has 5 FDA 510(k) cleared medical devices. Based in West Lafayette, US.

Historical record: 5 cleared submissions from 1994 to 1999. Primary specialty: Gastroenterology & Urology.

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

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

5 devices

1-5 of 5