Product code IXG— Radiology

BENNETT X-RAY HORIZ RADIO FLOAT/HI-LO ELEV TABLE

Classification name
Phantom, Anthropomorphic, Radiographic
Device class
Class 1
Regulation
21 CFR 892.1950
Advisory panel
Radiology
Total cleared
4
First cleared
Most recent

Market context for product code IXG

FDA has cleared 4 devices under product code IXG between 1984 and 1991, filed by 4 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 IXG

Recent clearances under product code IXG

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