GXS
- Product code
- GXS
- Device name
- Monitor, Alpha
- Device class
- Class 2
- 21 CFR
- 21 CFR 882.1610
- Medical specialty
- Neurology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
Official FDA classification page: GXS
Classification and pathway per current FDA publications. Data from openFDA (CC0).