DeviceClearance

Product code KEJ— Pathology

MICROSCOPE STAGE HEATER

Classification name
Stages, Microscope
Device class
Class 1
Regulation
21 CFR 864.3600
Advisory panel
Pathology
Total cleared
1
First cleared
Most recent

Market context for product code KEJ

FDA has cleared 1 device under product code KEJ, all in 1988, filed by 1 applicant company. 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.

Top applicants under product code KEJ

Recent clearances under product code KEJ

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