meddevicedb.com FDA Device Reference

MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159

K001698 Class II Traditional
Decision Date
2000-07-17
Sponsor / Applicant
Cogent Light Technologies, Inc.

Technical Specification

510(k) Submission ID K001698
Product Code FFS
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2000-07-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159 received FDA 510(k) clearance under submission number K001698, sponsored by Cogent Light Technologies, 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 2000-07-17.

Classification & Regulation

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