DeviceClearance

Product code ECG— Dental

BAR & RIDER, SCREWS, TUBES

Classification name
Sterilizer, Boiling Water
Device class
Class 1
Regulation
21 CFR 872.6710
Advisory panel
Dental
Total cleared
7
First cleared
Most recent

Market context for product code ECG

FDA has cleared 7 devices under product code ECG between 1977 and 1989, filed by 7 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 ECG

Recent clearances under product code ECG

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