510(k) K182122 ยท EYB Catheter, Ureteral, Gastro-Urology
Ureteric Catheters
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 4, 2018 |
| Received | Aug 6, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182122
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.