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EVIS EXERA COLONOVIDEOSCOPE MODEL XCF-Q160W1L/1

K043487 Class II Traditional
Decision Date
2005-01-28
Sponsor / Applicant
Aizu Olympus Co., Ltd.

Technical Specification

510(k) Submission ID K043487
Product Code FDF
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2005-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EVIS EXERA COLONOVIDEOSCOPE MODEL XCF-Q160W1L/1 received FDA 510(k) clearance under submission number K043487, sponsored by Aizu Olympus Co., Ltd.. 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 2005-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code FDF and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.