LGX
- Product code
- LGX
- Device name
- Table, Examination, Medical, Powered
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.4960
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 14
Official FDA classification page: LGX
Classification and pathway per current FDA publications. Data from openFDA (CC0).