Product code IZZ— Radiology

ALPHA

Classification name
Table, Radiographic, Non-Tilting, Powered
Device class
Class 2
Regulation
21 CFR 892.1980
Advisory panel
Radiology
Total cleared
29
First cleared
Most recent

Market context for product code IZZ

FDA has cleared 29 devices under product code IZZ between 1977 and 1997, filed by 22 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 IZZ

Recent clearances under product code IZZ

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