GWE
- Product code
- GWE
- Device name
- Stimulator, Photic, Evoked Response
- Device class
- Class 2
- 21 CFR
- 21 CFR 882.1890
- Medical specialty
- Neurology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 49
Official FDA classification page: GWE
Classification and pathway per current FDA publications. Data from openFDA (CC0).