LKG
- Product code
- LKG
- Device name
- Port & Catheter, Implanted, Subcutaneous, Intraventricular
- Device class
- Class 2
- 21 CFR
- 21 CFR 882.5550
- Medical specialty
- Neurology
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (last 3 years)
- 8
Official FDA classification page: LKG
Classification and pathway per current FDA publications. Data from openFDA (CC0).