# K024126: Clear or Braided Contrast Media Injection Line or Without Rotator, Cath Lab Kit

- Pathway: 510(k) (Special)
- Applicant: Abbott Laboratories
- Decided: Jan 14, 2003 after 29 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
High Pressure Tubing (intravascular administration set) intended use Indicated as 10” (or up to 48”) CLEAR (or BRAIDED) CONTRAST‘ MEDIA INJECTION LINE WITH ROTATOR, for use in Cardiac catheterization and radiology special procedure

Source page: https://510kreport.com/device/K024126
Methodology: https://510kreport.com/methodology