# K260737: Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Female (CH06 - CH16); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Straight (CH06 - CH18); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Coude (CH10 - CH18).

- Pathway: 510(k) (Traditional)
- Applicant: Convatec
- Decided: Aug 5, 2026 after 152 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: 5 generations back to K896729 (1990). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132500: Cure Catheter Female, Cure Catheter Male, Cure Catheter Coude, Cure Catheter Pediatric, Cure Catheter Hydrophilic Coated, Cure Medical, LLC (2013) Summary page 5.

## Indications for use
The Cure Aqua Ready to Use Hydrophilic Intermittent Catheter is an intermittent urinary catheter that is inserted through the urethra and indicated for the purpose of bladder drainage.

Source page: https://510kreport.com/device/K260737
Methodology: https://510kreport.com/methodology