Product code LRB— Ear, Nose, Throat

AIR CONDUCTION IN-THE-EAR HEARING AID UA/115/SCR

Classification name
Face Plate Hearing Aid
Device class
Class 1
Regulation
21 CFR 874.3300
Advisory panel
Ear, Nose, Throat
Total cleared
24
First cleared
Most recent

Market context for product code LRB

FDA has cleared 24 devices under product code LRB between 1984 and 1998, filed by 11 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 LRB

Recent clearances under product code LRB

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