Product code KGZ— General, Plastic Surgery

3-WAY STOPCOCK WITH LUER-LOCK FITTING

Classification name
Accessories, Catheter
Device class
Class 1
Regulation
21 CFR 878.4200
Advisory panel
General, Plastic Surgery
Total cleared
29
First cleared
Most recent

Market context for product code KGZ

FDA has cleared 29 devices under product code KGZ between 1976 and 2002, filed by 23 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

last 15 years

Top applicants under product code KGZ

Recent clearances under product code KGZ

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