MUW
- Product code
- MUW
- Device name
- Lens, Contact (Orthokeratology)
- Device class
- Class 2
- 21 CFR
- 21 CFR 886.5916
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K)
- 510(k) clearances (all years, FDA)
- 6 (all years; only the last 3 years are listed here)
Official FDA classification page: MUW
Classification and pathway per current FDA publications. Data from openFDA (CC0).