# K142745: 125mL CT Syringe

- Pathway: 510(k) (Traditional)
- Applicant: Coeur, Inc.
- Decided: Apr 1, 2015 after 189 days
- Product code: DXT (Injector And Syringe, Angiographic)
- Device class: 2
- Regulation: 21 CFR 870.1650
- 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 K971712 (1997). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K971712: Coeur 130 ML Angiographic Syringe, Coeur Laboratories, Inc. (1997) Summary page 4.

## Indications for use
For use with the Liebel-Flarsheim Optivantage and Liebel-Flarsheim CT 9000 ADV Injectors for the injection of contrast media or saline.

Source page: https://510kreport.com/device/K142745
Methodology: https://510kreport.com/methodology