Product code LJW— Ear, Nose, Throat

EMERGENCY TRACHEOSTOMY INSTRUMENT SET

Classification name
Tracheotome
Device class
Class 1
Regulation
21 CFR 874.4420
Advisory panel
Ear, Nose, Throat
Total cleared
2
First cleared
Most recent

Market context for product code LJW

FDA has cleared 2 devices under product code LJW between 1983 and 1994, filed by 2 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 LJW

Recent clearances under product code LJW

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