EKE
- Product code
- EKE
- Device name
- Curette, Operative
- Device class
- Class 1
- 21 CFR
- 21 CFR 872.4565
- Medical specialty
- Dental
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: EKE
Classification and pathway per current FDA publications. Data from openFDA (CC0).