DeviceClearance

Product code EQH— Ear, Nose, Throat

ASPIRATING ENDO OCULAR PROBE

Classification name
Source, Carrier, Fiberoptic Light
Device class
Class 1
Regulation
21 CFR 874.4350
Advisory panel
Ear, Nose, Throat
Total cleared
49
First cleared
Most recent

Market context for product code EQH

FDA has cleared 49 devices under product code EQH between 1976 and 1995, filed by 26 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 EQH

Recent clearances under product code EQH

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