510(k) K201165 ยท LJE Catheter, Nephrostomy
In-Ka Percutaneous Balloon Dilatation Catheters, Amplatz Sheath
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Unknown, Dec 17, 2020 |
| Received | May 1, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201165
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.