Product code IXC— Radiology

ADVIEWER 2000

Classification name
Illuminator, Radiographic-Film
Device class
Class 1
Regulation
21 CFR 892.1890
Advisory panel
Radiology
Total cleared
18
First cleared
Most recent

Market context for product code IXC

FDA has cleared 18 devices under product code IXC between 1980 and 1999, filed by 16 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 IXC

Recent clearances under product code IXC

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