Product code MYD— Ophthalmic
VISIJET HYDROKERATOME, MODEL 50
- Classification name
- Keratome, Water Jet
- Device class
- Class 1
- Regulation
- 21 CFR 886.4370
- Advisory panel
- Ophthalmic
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code MYD
FDA has cleared device under product code MYD, all in 2000, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Top applicants under product code MYD
Recent clearances under product code MYD
Data sourced from openFDA. This site is unofficial and independent of the FDA.