EAK
- Product code
- EAK
- Device name
- Screen, Leaded, Operator Radiation Protector
- Device class
- Class 1
- 21 CFR
- 21 CFR 892.6500
- Medical specialty
- Radiology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 7
Official FDA classification page: EAK
Classification and pathway per current FDA publications. Data from openFDA (CC0).