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FORMULA 418 BILIARY STENT

K051785 Class II Traditional
Decision Date
2005-08-23
Sponsor / Applicant
Cook, Inc.

Technical Specification

510(k) Submission ID K051785
Product Code FGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5010
Decision Date 2005-08-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FORMULA 418 BILIARY STENT received FDA 510(k) clearance under submission number K051785, sponsored by Cook, 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 2005-08-23.

Classification & Regulation

This clearance is catalogued under FDA product code FGE and 21 CFR 876.5010, within the Gastroenterology, Urology review panel as a Class II device.