Medical Device Manufacturer · US , Redwood City , CA

Proteus Biomedical, Inc. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 2010

Total

Cleared

Denied

Proteus Biomedical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Redwood City, US.

Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Proteus Biomedical, Inc.

2 devices

1-2 of 2