HJJ
- Product code
- HJJ
- Device name
- Lens, Fresnel, Flexible, Diagnostic
- Device class
- Class 1
- 21 CFR
- 21 CFR 886.1390
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K) Exempt
- Flag
- GMP exempt
Official FDA classification page: HJJ
Classification and pathway per current FDA publications. Data from openFDA (CC0).