# K023514: Trellis-6 Peripheral Infusion System (140CM Catheter Length 10CM Infusion Length)

- Pathway: 510(k) (Traditional)
- Applicant: Bacchus Vascular, Inc.
- Decided: Dec 2, 2002 after 42 days
- Product code: QEY (Mechanical Thrombolysis Catheter)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K904788 (1990). 9 ancestors in all.
56 later devices descend from it; 2 cite it directly.
2 of 66 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013635: Trellis Infusion System (10CM Infusion Length); Trellis Infusion System (20CM Infusion Length), Bacchus Vascular, Inc. (2002)
- K021958: Trellis Plus Infusion System (140CM Catheter Length 10CM Infusion Length 20CM (100CM Catheter Length 10CM Infusion H, Bacchus Vascular, Inc. (2002) Summary page 7.

## Most influential descendants
- K030637: Ekos Peripheral Infusion System (2003), 50 descendants of its own
- K033214: Ekos Peripheral Infusion System (2003), 46 descendants of its own
- K041629: Lysus Infusion System (2004), 39 descendants of its own
- K042456: Lysus Infusion System (2004), 38 descendants of its own
- K051319: Lysus Infusion System (2005), 35 descendants of its own

## Recalls of this device
- Nov 24, 2003 · Not classified · Z-0817-04: The device has the potential for fractures at the distal end during use.

## Indications for use
The TrellisTMReserve Infusion System is intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature.

Source page: https://510kreport.com/device/K023514
Methodology: https://510kreport.com/methodology