Kerberos Proximal Solutions, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kerberos Proximal Solutions, Inc. - FDA 510(k) Cleared Devices
5
Total
2
Cleared
0
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.
FDA 510(k) Regulatory Record - Kerberos Proximal Solutions, Inc.
5 devices
Cleared
Sep 20, 2006
RINSPIRATION CATHETER SYSTEM, MODELS 50135, 550135, P7065, P70135
Cardiovascular
44d
Cleared
May 13, 2005
KERBEROS PROXIMAL SOLUTIONS RISPIRATION SYSTEM
Cardiovascular
112d
Cleared
Aug 26, 2004
RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703
Cardiovascular
118d
Cleared
Jul 22, 2004
KERBEROS OCCLUDING GUIDE CATHETER AND ACCESSORIES
Cardiovascular
80d
Cleared
May 21, 2004
RINSPIRATION SYSTEM
Cardiovascular
7d