# K060074: Interlink System-T-Connector Extension Set, Model 2N3326

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corp
- Decided: Mar 29, 2006 after 78 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: 1 generation back to K921899 (1993). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K921899: Interlink System - T-Connector Extension Set, Baxter Healthcare Corp (1993) Summary page 1.

## Most influential descendants
- K112799: Med-RX Extension Set with T-Connector (2011), 0 descendants of its own

## Indications for use
For use in neonatal population only. To be used with an indwelling catheter for the administration or withdrawal of fluids. This device may aid in the prevention of needlestick injuries.

Source page: https://510kreport.com/device/K060074
Methodology: https://510kreport.com/methodology