meddevicedb.com FDA Device Reference

SLIM LINE RETENT TIP W/SILICONE INFLATION CUFF

K904299 Class II Traditional
Decision Date
1990-11-27
Sponsor / Applicant
E-Z-Em, Inc.

Technical Specification

510(k) Submission ID K904299
Product Code FGD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 1990-11-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SLIM LINE RETENT TIP W/SILICONE INFLATION CUFF received FDA 510(k) clearance under submission number K904299, sponsored by E-Z-Em, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1990-11-27.

Classification & Regulation

This clearance is catalogued under FDA product code FGD and 21 CFR 876.5980, within the Gastroenterology, Urology review panel as a Class II device.