DeviceClearance

Product code IZG— Radiology

DISCOGRAPHY KIT

Classification name
System, X-Ray, Photofluorographic
Device class
Class 2
Regulation
21 CFR 892.1730
Advisory panel
Radiology
Total cleared
7
First cleared
Most recent

Market context for product code IZG

FDA has cleared 7 devices under product code IZG between 1989 and 1996, filed by 7 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

Top applicants under product code IZG

Recent clearances under product code IZG

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