# K241851: Versus™ Catheter  (VS110-8B)

- Pathway: 510(k) (Traditional)
- Applicant: Liquet Medical, Inc.
- Decided: Nov 25, 2024 after 151 days
- Product code: QEY (Mechanical Thrombolysis Catheter)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 19 generations back to K904788 (1990). 62 ancestors in all.
1 later device descends from it; 1 cites it directly.
1 of 64 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183290: Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200, Thrombolex, Inc. (2019) Summary page 5.
- K160084: Swan Ganz Catheters, Edwards Lifesciences, LLC (2016) Summary page 5.

## Most influential descendants
- K260149: Versus™ Catheter  (VS110-9NB) (2026), 0 descendants of its own

## Indications for use
The Versus™ Catheter is indicated for: The controlled and selective infusion of physician-specified fluids, including thrombolytics, into the pulmonary artery vasculature in adult patients. The assessment of a patient’s hemodynamic condition through direct intracardiac and pulmonary artery pressure monitoring.

Source page: https://510kreport.com/device/K241851
Methodology: https://510kreport.com/methodology