# K222279: Rusch Intermittent Urethral Catheters

- Pathway: 510(k) (Special)
- Applicant: Teleflex Medical
- Decided: Aug 29, 2022 after 31 days
- Product code: EZC (Catheter, Coude)
- 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: 1 generation back to K173596 (2018). 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)
- K173596: Rusch Intermittent Urethral Catheters, Teleflex Medical (2018) Summary page 4.

## 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.

Source page: https://510kreport.com/device/K222279
Methodology: https://510kreport.com/methodology