510(k) K260737 · EZD Catheter, Straight
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).
| Applicant | Convatec, Flintshire, GB |
| Decision | Substantially Equivalent, Aug 5, 2026 |
| Received | Mar 6, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260737
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.