# K261766: CPS Locator 3D Plus Delivery Catheter

- Pathway: 510(k) (Special)
- Applicant: CenterPoint Systems, LLC
- Decided: Jul 29, 2026 after 62 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: 13 generations back to K893658 (1989). 60 ancestors in all.
No later device cites it as a predicate yet.
0 of 61 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K250828: CPS Locator 3D Plus Delivery Catheter, CenterPoint Systems, LLC (2025) Summary page 5.

## Indications for use
The Delivery Catheter is indicated for the introduction of various types of pacing or defibrillator leads to the right heart, inclusive of the Left Bundle Branch Area.

Source page: https://510kreport.com/device/K261766
Methodology: https://510kreport.com/methodology