Product code EBR— Dental

A-DEC 7284 CUSPIDOR, CASCADE

Classification name
Unit, Suction Operatory
Device class
Class 1
Regulation
21 CFR 872.6640
Advisory panel
Dental
Total cleared
3
First cleared
Most recent

Market context for product code EBR

FDA has cleared 3 devices under product code EBR between 1977 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 EBR

Recent clearances under product code EBR

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