EAS
- Product code
- EAS
- Device name
- Gel, Electrode, For Pulp Tester
- Device class
- Class 1
- 21 CFR
- 21 CFR 872.1730
- Medical specialty
- Dental
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: EAS
Classification and pathway per current FDA publications. Data from openFDA (CC0).