GWR
- Product code
- GWR
- Device name
- Generator, Electroencephalograph Test Signal
- Device class
- Class 1
- 21 CFR
- 21 CFR 882.1430
- Medical specialty
- Neurology
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: GWR
Classification and pathway per current FDA publications. Data from openFDA (CC0).