Product code HOF— Ophthalmic
VISI-WIPE
- Classification name
- Burr, Corneal, Manual
- Device class
- Class 1
- Regulation
- 21 CFR 886.4350
- Advisory panel
- Ophthalmic
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code HOF
FDA has cleared device under product code HOF, all in 1989, 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 HOF
Recent clearances under product code HOF
Data sourced from openFDA. This site is unofficial and independent of the FDA.