510(k) K233101 ยท EZD Catheter, Straight
Luja Coude (20108 Male CH18 - large packaging)
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 26, 2023 |
| Received | Sep 26, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233101
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.