Medical Device Manufacturer · US , Cupertino , CA

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

3 submissions · 3 cleared · Since 2007

Total

Cleared

Denied

Bioimagene, Inc. has 3 FDA 510(k) cleared medical devices. Based in Cupertino, US.

Historical record: 3 cleared submissions from 2007 to 2010. Primary specialty: Pathology.

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

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

3 devices

1-3 of 3