510(k) K211911 ยท LJE Catheter, Nephrostomy
Kolibri Percutaneous Nephrostomy Catheters, Kolibri Percutaneous Nephrostomy Kits, Kolibri Direct Puncture Sets
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Unknown, Mar 10, 2022 |
| Received | Jun 21, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211911
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.