DeviceClearance

Product code HOD— Ophthalmic

BURTON AUTOMATIC PROJECTOR - MODEL CP-40

Classification name
Clamp, Eyelid, Ophthalmic
Device class
Class 1
Regulation
21 CFR 886.4350
Advisory panel
Ophthalmic
Total cleared
3
First cleared
Most recent

Market context for product code HOD

FDA has cleared 3 devices under product code HOD between 1983 and 1993, filed by 3 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 HOD

Recent clearances under product code HOD

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