Product code FKC— Gastroenterology, Urology

CANNULA CLAMP

Classification name
Clamp, Cannula
Device class
Class 1
Regulation
21 CFR 876.5540
Advisory panel
Gastroenterology, Urology
Total cleared
1
First cleared
Most recent

Market context for product code FKC

FDA has cleared 1 device under product code FKC, all in 1977, 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 FKC

Recent clearances under product code FKC

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