DeviceClearance

Product code HQH— Ophthalmic

CUSTOM ARTIFICIAL HUMAN EYES

Classification name
Eye, Artificial, Non-Custom
Device class
Class 1
Regulation
21 CFR 886.3200
Advisory panel
Ophthalmic
Total cleared
6
First cleared
Most recent

Market context for product code HQH

FDA has cleared 6 devices under product code HQH between 1980 and 1995, filed by 6 applicant companies. 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.

Clearances per year

Top applicants under product code HQH

Recent clearances under product code HQH

Data sourced from openFDA. This site is unofficial and independent of the FDA.