LJE
- Product code
- LJE
- Device name
- Catheter, Nephrostomy
- Device class
- Class U
- Medical specialty
- Unknown
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 1
- Summaries archived here
- 1 (direct download)
- 510(k) clearances (all years, FDA)
- 56 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K250448 | 2025-07-03 | Shenzhen Trious Medical Technology Co.… | Disposable Percutaneous Nephrostomy Dilatation Kit |
Official FDA classification page: LJE
Classification and pathway per current FDA publications. Data from openFDA (CC0).