DeviceClearance

Product code KZF— General Hospital

ABCO EXAMINATION LAMP (GOOSENECK TYPE)

Classification name
Device, Medical Examination, Ac Powered
Device class
Class 1
Regulation
21 CFR 880.6320
Advisory panel
General Hospital
Total cleared
37
First cleared
Most recent

Market context for product code KZF

FDA has cleared 37 devices under product code KZF between 1978 and 1996, filed by 18 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 KZF

Recent clearances under product code KZF

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