# K253741: V•Stick™ Vascular Access Set

- Pathway: 510(k) (Special)
- Applicant: Argon Medical Devices, Inc.
- Decided: Dec 15, 2025 after 21 days
- Product code: DYB (Introducer, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1340
- 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 K031691 (2003). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130730: V-Stick Vascular Access Set, Argon Medical (2013) Summary page 5.

## Indications for use
The V•Stick™ Vascular Access Set is intended for use in the introduction and placement of guidewires and/or catheters.

Source page: https://510kreport.com/device/K253741
Methodology: https://510kreport.com/methodology