# K190475: Delivery Catheter SSPC1, Delivery Catheter SSPC2, Delivery Catheter SSPC3, Delivery Catheter SSPC4

- Pathway: 510(k) (Traditional)
- Applicant: Centerpoint Systems
- Decided: Jun 28, 2019 after 121 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: 10 generations back to K893658 (1989). 57 ancestors in all.
5 later devices descend from it; 2 cite it directly.
0 of 63 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101885: Medtronic C315 Delivery Catheter, Medtronic, Inc. (2010) Summary page 4.

## Most influential descendants
- K230363: CPS Locator 3D Delivery Catheter (2023), 3 descendants of its own
- K250828: CPS Locator 3D Plus Delivery Catheter (2025), 1 descendant of its own
- K261766: CPS Locator 3D Plus Delivery Catheter (2026), 0 descendants of its own
- K250147: CPS Locator 3D Delivery Catheter (2025), 0 descendants of its own
- K250492: FlexiGo 3D Delivery Catheter (2025), 0 descendants of its own

## Indications for use
The Delivery Catheter is indicated for the introduction of various types of catheters and pacing or defibrillator leads.

Source page: https://510kreport.com/device/K190475
Methodology: https://510kreport.com/methodology