# K202610: Ventrax Delivery System

- Pathway: 510(k) (Traditional)
- Applicant: Merit Medical Systems, Inc.
- Decided: Dec 14, 2020 after 96 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: 7 generations back to K893658 (1989). 39 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 42 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072313: Amplatzer Torqvue Delivery System, Aga Medical Corp. (2007) Summary page 4.

## Most influential descendants
- K231246: Ventrax™ Delivery System  (VTR851) (2023), 1 descendant of its own
- K242873: Ventrax™ Delivery System (2025), 0 descendants of its own

## Indications for use
The Ventrax Delivery System is intended to provide a pathway through which devices are introduced within the chambers and coronary vasculature of the heart

Source page: https://510kreport.com/device/K202610
Methodology: https://510kreport.com/methodology