HLX
- Product code
- HLX
- Device name
- Photostimulator, Ac-Powered
- Device class
- Class 2
- 21 CFR
- 21 CFR 886.1630
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 18
Official FDA classification page: HLX
Classification and pathway per current FDA publications. Data from openFDA (CC0).