# K120781: Cello Balloon Guide Catheter (6F), 950 MM and 1020 MM Length

- Pathway: 510(k) (Traditional)
- Applicant: Fuji Systems Corp.
- Decided: Aug 9, 2012 after 147 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). 2 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 7 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.

## Most influential descendants
- K203723: Branchor Balloon Guide Catheter (2021), 2 descendants of its own
- K221951: Branchor Balloon Guide Catheter (2022), 1 descendant of its own
- K251240: Branchor X Balloon Guide Catheter (2025), 0 descendants of its own
- K223275: CELLO II Balloon Guide Catheter (2022), 0 descendants of its own

## Indications for use
The CELLO Balloon Guide Catheter is indicated for use in facilitating the insertion and guidance of intravascular catheters into a selected blood vessel in the peripheral and neurovasculature systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures.

Source page: https://510kreport.com/device/K120781
Methodology: https://510kreport.com/methodology