DeviceClearance

Product code KXJ— Radiology

ALLMEC 90/15

Classification name
Table, Radiologic
Device class
Class 2
Regulation
21 CFR 892.1980
Advisory panel
Radiology
Total cleared
31
First cleared
Most recent

Market context for product code KXJ

FDA has cleared 31 devices under product code KXJ between 1978 and 2005, filed by 26 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

last 15 years

Top applicants under product code KXJ

Recent clearances under product code KXJ

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