# K150513: Imed Technology Intravascular Administration Set, Imed Technology Extension Set

- Pathway: 510(k) (Abbreviated)
- Applicant: Imed Technology, Inc.
- Decided: May 28, 2015 after 90 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: 4 generations back to K925465 (1993). 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)
- K121803: Intravascular Administration Set, Acta Medical, LLC (2012) Summary page 4.

## Indications for use
IMed Technology Intravascular administration set and Imed Technology Extension sets intended use is to deliver sterile, infusion fluid from a container to the patient with or without flow control features. IMed Technology infusion tubing may act as an extension of other infusion tubing in delivering intravenous fluids from a container to patient.

Source page: https://510kreport.com/device/K150513
Methodology: https://510kreport.com/methodology