DeviceClearance

Product code KYT— General Hospital

C-LITE

Classification name
Light, Examination, Medical, Battery Powered
Device class
Class 1
Regulation
21 CFR 880.6350
Advisory panel
General Hospital
Total cleared
6
First cleared
Most recent

Market context for product code KYT

FDA has cleared 6 devices under product code KYT between 1977 and 1992, filed by 5 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 KYT

Recent clearances under product code KYT

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