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: Cardiovascular.

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

Proteus Biomedical, 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 - Proteus Biomedical, Inc.

2 devices

1-2 of 2