# K261418: Liquick X-treme, Liquick X-treme Plus

- Pathway: 510(k) (Traditional)
- Applicant: Teleflex Medical
- Decided: Sep 23, 2026 after 146 days
- Product code: EZD (Catheter, Straight)
- Device class: 2
- Regulation: 21 CFR 876.5130
- 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 K000070 (2000). 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)
- K183461: Rusch Flocath Hydrophilic Intermittent Catheter, Rusch MMG Hydrophilic Intermittent Catheter, Teleflexmedical, Inc. (2019) Summary page 5.

## Indications for use
These catheters are indicated for the routine drainage of urine from the bladder. These catheters are not intended or designed for indwelling use. Catheters are indicated for use in male and female adults and pediatric patients in the following pediatric subgroups: Children (2 years old to less than 12 years old), Adolescents (12 years old to less than 18 years old), and Transitional Adolescents (18 years old to less than 22 years old but treated like adult).

Source page: https://510kreport.com/device/K261418
Methodology: https://510kreport.com/methodology