# K222679: Vericor Support Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Vascupatent Medical (Shenzhen) Co., Ltd.
- Decided: Nov 7, 2022 after 62 days
- Product code: KRA (Catheter, Continuous Flush)
- Device class: 2
- Regulation: 21 CFR 870.1210
- 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 K052841 (2005). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K160884: CXI Support Catheter, Cook Incorporated (2016) Summary page 5.

## Indications for use
The Vericor Support Catheter is intended for use in small vessel or superselective anatomy for diagnostic and interventional procedures, including peripheral use.

Source page: https://510kreport.com/device/K222679
Methodology: https://510kreport.com/methodology