DeviceClearance

Product code KGK— Anesthesiology

GAS COLLHCTOR BE 155(155-2-3,154-4)

Classification name
Gas, Collecting Vessel
Device class
Class 1
Regulation
21 CFR 868.1575
Advisory panel
Anesthesiology
Total cleared
2
First cleared
Most recent

Market context for product code KGK

FDA has cleared 2 devices under product code KGK between 1977 and 1986, filed by 2 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 KGK

Recent clearances under product code KGK

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