Product code EYK— Gastroenterology, Urology

URETERAL CATHETER AND ACCESSORIES

Classification name: Connector, Ureteral Catheter
Device class: Class 1
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Total cleared: 1
First cleared: 1994-05-25
Most recent: 1994-05-25

Market context for product code EYK

FDA has cleared 1 device under product code EYK, all in 1994, 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 EYK

Urological Associates of Central Jersey P.A.1 clearance

Recent clearances under product code EYK

K934419 — URETERAL CATHETER AND ACCESSORIESUrological Associates of Central Jersey P.A.·1994-05-25

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