# K112799: Med-RX Extension Set with T-Connector

- Pathway: 510(k) (Traditional)
- Applicant: Benlan, Inc.
- Decided: Dec 23, 2011 after 87 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: 2 generations back to K921899 (1993). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060074: Interlink System-T-Connector Extension Set, Model 2N3326, Baxter Healthcare Corp (2006) Summary page 1.

## Indications for use
The MED-RX Extension Set with T-Connector is intended to be used for administration or withdrawal of fluids to or from a neonatal patient as directed by a physician.

Source page: https://510kreport.com/device/K112799
Methodology: https://510kreport.com/methodology