510(k) K241210 ยท EZD Catheter, Straight
Luja Coude
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Nov 21, 2024 |
| Received | Apr 30, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241210
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.