DeviceClearance

Product code KZA— General Hospital

E-Z-JECTOR

Classification name
Device, Vein Location, Liquid Crystal
Device class
Class 1
Regulation
21 CFR 880.6970
Advisory panel
General Hospital
Total cleared
6
First cleared
Most recent

Market context for product code KZA

FDA has cleared 6 devices under product code KZA between 1978 and 2016, filed by 5 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 KZA

Recent clearances under product code KZA

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