HRE
- Product code
- HRE
- Device name
- Cabinet, Instrument, Ac-Powered, Ophthalmic
- Device class
- Class 1
- 21 CFR
- 21 CFR 886.1860
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: HRE
Classification and pathway per current FDA publications. Data from openFDA (CC0).