Product code EHO— Dental

70-X/RVG (RADIOVISIOGRAPHY)

Classification name
Bar, Preformed
Device class
Class 1
Regulation
21 CFR 872.3165
Advisory panel
Dental
Total cleared
3
First cleared
Most recent

Market context for product code EHO

FDA has cleared 3 devices under product code EHO between 1988 and 1994, 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 EHO

Recent clearances under product code EHO

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