HJS
- Product code
- HJS
- Device name
- Test, Spectacle Dissociation, Ac-Powered (Lancaster)
- Device class
- Class 1
- 21 CFR
- 21 CFR 886.1910
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: HJS
Classification and pathway per current FDA publications. Data from openFDA (CC0).