LNK
- Product code
- LNK
- Device name
- Laser For Gastro-Urology Use
- Device class
- Class 2
- 21 CFR
- 21 CFR 878.4810
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 60
Official FDA classification page: LNK
Classification and pathway per current FDA publications. Data from openFDA (CC0).