# K073260: Liisa Lever Integrated Interventional System Adapter, Model VSL-109

- Pathway: 510(k) (Abbreviated)
- Applicant: Device Partners International
- Decided: Mar 13, 2008 after 114 days
- Product code: DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4290
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K854261 (1985). 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)
- K991102: Copilot Bleedback Control Valve, Model 1003331, Guidant Corp. (1999) Summary page 1.
- K060759: Y-Click Connector, Elcam Medical Acal (2006) Summary page 1.

## Indications for use
The LiiSA Lever Integrated Interventional System AdaptorTM is a Y-Connector and hemostasis valve which is intended to maintain hemostasis during the introduction, use and withdrawal of diagnostic or interventional devices (i.e., guide wires, balloon catheters, stents) used in angioplasty procedures. It is compatible with guiding catheters 9 F or smaller and 0.014" - 0.038" guide wires.

Source page: https://510kreport.com/device/K073260
Methodology: https://510kreport.com/methodology