LKX
- Product code
- LKX
- Device name
- Device, Thermal, Hemorrhoids
- Device class
- Class U
- Medical specialty
- Unknown
- Marketing pathway
- 510(K)
- 510(k) clearances (all years, FDA)
- 18 (all years; only the last 3 years are listed here)
Official FDA classification page: LKX
Classification and pathway per current FDA publications. Data from openFDA (CC0).