GZN
- Product code
- GZN
- Device name
- Rheoencephalograph
- Device class
- Class 3
- 21 CFR
- 21 CFR 882.1825
- Medical specialty
- Neurology
- Marketing pathway
- PMA
FDA classification definition
Call for PMAs to be filed by 12/26/96 per 61 FR 50708 on 9/27/96
Official FDA classification page: GZN
Classification and pathway per current FDA publications. Data from openFDA (CC0).