# K150970: Coda LP Balloon Catheter

- Pathway: 510(k) (Special)
- Applicant: Cook Incorporated
- Decided: May 12, 2015 after 29 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: 3 generations back to K003495 (2001). 4 ancestors in all.
10 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032869: Cook Coda Balloon Catheter, Cook, Inc. (2003) Summary page 4.
- K122917: Coda Balloon Catheter, Cook, Inc. (2013) Summary page 4.

## Most influential descendants
- K151821: ER-REBOA Catheter (2015), 9 descendants of its own
- K170411: ER-REBOA Catheter (2017), 8 descendants of its own
- K172790: ER-REBOA Catheter (2017), 4 descendants of its own
- K210358: Neurescue device (2021), 1 descendant of its own
- K200459: pREBOA-PRO Catheter (2020), 1 descendant of its own

## Indications for use
The Coda® LP Balloon Catheter is intended for the temporary occlusion of large vessels, or to expand vascular prostheses.

Source page: https://510kreport.com/device/K150970
Methodology: https://510kreport.com/methodology