510(k) K201007 ยท EZN Dilator, Catheter, Ureteral
In-Ka Ureteral Balloon Dilatation Catheter
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Unknown, Jun 11, 2020 |
| Received | Apr 17, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201007
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.