# K222780: LILY Extension Tube and Needleless Connector

- Pathway: 510(k) (Traditional)
- Applicant: Lily Medical Corporation
- Decided: Nov 9, 2023 after 421 days
- Product code: FPA (Set, Administration, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5440
- 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 K942988 (1995). 17 ancestors in all.
No later device cites it as a predicate yet.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140831: Maxzero Extension Set with Needless Connector, Care Fusion (2014) Summary page 5.

## Indications for use
The LILY Extension Tube and Needleless Connector is a sterile single patient use device for the administration of fluids from a container into the patient’s vascular system through a vascular access device. It is for direct injection, continuous or intermittent infusion, aspiration and needle-free delivery of solutions during IV therapy.

Source page: https://510kreport.com/device/K222780
Methodology: https://510kreport.com/methodology