Medical Device Manufacturer · US , Mountain View , CA

Kerberos Proximal Solutions, Inc. - FDA 510(k) Cleared Devices

5 submissions · 2 cleared · Since 2004

Total

Cleared

Denied

Kerberos Proximal Solutions, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mountain View, US.

Historical record: 2 cleared submissions from 2004 to 2006. Primary specialty: Cardiovascular.

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

Kerberos Proximal Solutions, Inc. is one of 24545 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kerberos Proximal Solutions, Inc.

5 devices

1-5 of 5