# K041151: Kerberos Occluding Guide Catheter and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Kerberos Proximal Solutions, Inc.
- Decided: Jul 22, 2004 after 80 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K010954 (2001). 7 ancestors in all.
25 later devices descend from it; 1 cites it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K021899: Concentric Balloon Guide Catheter, Model 90072, Concentric Medical, Inc. (2002) Summary page 1.
- K002286: Ldob Occlusion Balloon Catheter, Cook, Inc. (2001) Summary page 1.
- K033441: Boston Scientific 6F Runway Guide Catheter, Boston Scientific Corp (2003) Summary page 1.
- K984214: Cordis Endovascular Temporary Occlusion Balloon Catheter, Cordis Neurovascular, Inc. (1999) Summary page 1.
- K973298: Cardima Vueport Coronary Sinus Balloon Occlusion Guiding Catheter, Cardima, Inc. (1998) Summary page 1.

## Most influential descendants
- K080987: Bridgepoint Medical Stingray Device and Accessories (2009), 24 descendants of its own
- K101591: Stingray Orienting Balloon Catheter (2010), 14 descendants of its own
- K102725: Crossboss Catheter Model M-2000, Stingray Orienting Balloon Catheter Model M-1000, Stingray Guidewire Model M-3004 and M (2011), 11 descendants of its own
- K121763: Multicross Support Catheter (2012), 8 descendants of its own
- K111963: Bridgepoint Medical Mantaray (TM) Catheter (2011), 7 descendants of its own

## Indications for use
The Kerberos Proximal Solutions Occluding Guide Catheter (OCG) and Accessories are intended to facilitate the use and guidance of intravascular catheters into selected blood vessels in the peripheral, cardiovascular and neurovascular systems. The balloon provides temporary vascular occlusion during these percutaneous procedures.

Source page: https://510kreport.com/device/K041151
Methodology: https://510kreport.com/methodology
