# K903777: WRP Foleycath

- Pathway: 510(k) (Traditional)
- Applicant: Wembley Rubber Products (M) Sdn Bhd
- Decided: Dec 13, 1990 after 115 days
- Product code: EZL (Catheter, Retention Type, Balloon)
- 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
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K071423: Medline Latex Foley Catheter (2007), 4 descendants of its own
- K173340: Yikang Latex Foley Catheter (2018), 2 descendants of its own
- K232469: Rüsch Latex Gold Foley Catheter (2024), 1 descendant of its own
- K262056: Rusch Latex Gold Foley Catheter (2026), 0 descendants of its own
- K170233: Diposable Urinary Catheter (PVC Urinary Catheter, Silicone Urinary Catheter, Latex Urinary Catheter) (2017), 0 descendants of its own

Source page: https://510kreport.com/device/K903777
Methodology: https://510kreport.com/methodology