MYD
- Product code
- MYD
- Device name
- Keratome, Water Jet
- Device class
- Class 1
- 21 CFR
- 21 CFR 886.4370
- Medical specialty
- Ophthalmic
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (all years, FDA)
- 1 (all years; only the last 3 years are listed here)
Official FDA classification page: MYD
Classification and pathway per current FDA publications. Data from openFDA (CC0).