FXE
- Product code
- FXE
- Device name
- Speculum, Non-Illuminated
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.1800
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: FXE
Classification and pathway per current FDA publications. Data from openFDA (CC0).