DeviceClearance

Product code JGJ— Clinical Chemistry

MAGNESIUM

Classification name
Photometric Method, Magnesium
Device class
Class 1
Regulation
21 CFR 862.1495
Advisory panel
Clinical Chemistry
Total cleared
90
First cleared
Most recent

Market context for product code JGJ

FDA has cleared 90 devices under product code JGJ between 1977 and 2018, filed by 64 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

last 15 years

Top applicants under product code JGJ

Recent clearances under product code JGJ

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