EAM
- Product code
- EAM
- Device name
- Screen, Intensifying, Radiographic
- Device class
- Class 1
- 21 CFR
- 21 CFR 892.1960
- Medical specialty
- Radiology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 35 (all years; only the last 3 years are listed here)
Official FDA classification page: EAM
Classification and pathway per current FDA publications. Data from openFDA (CC0).