LLN
- Product code
- LLN
- Device name
- Device, Vibration Threshold Measurement
- Device class
- Class 1
- 21 CFR
- 21 CFR 882.1200
- Medical specialty
- Neurology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 13
Official FDA classification page: LLN
Classification and pathway per current FDA publications. Data from openFDA (CC0).