Product code LJL— General Hospital

LOUSEBUSTER

Classification name
Detectors And Removers, Lice, (Including Combs)
Device class
Class 1
Regulation
21 CFR 880.5960
Advisory panel
General Hospital
Total cleared
11
First cleared
Most recent

Market context for product code LJL

FDA has cleared 11 devices under product code LJL between 1982 and 2017, filed by 9 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 LJL

Recent clearances under product code LJL

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