DeviceClearance

Product code HQZ— Ophthalmic

SPECTACLE FRAMES

Classification name
Frame, Spectacle
Device class
Class 1
Regulation
21 CFR 886.5842
Advisory panel
Ophthalmic
Total cleared
198
First cleared
Most recent

Market context for product code HQZ

FDA has cleared 198 devices under product code HQZ between 1977 and 1995, filed by 179 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

last 15 years

Top applicants under product code HQZ

Recent clearances under product code HQZ

1–100 of 198

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