meddevicedb.com FDA Device Reference

HX-5/6-1 ENDOSCOPIC CLIPPING DEVICE, ENDOSCOPIC CLIPS

K990687 Class II Traditional
Decision Date
1999-03-26
Sponsor / Applicant
Olympus Optical, Co.

Technical Specification

510(k) Submission ID K990687
Product Code PKL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4400
Decision Date 1999-03-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HX-5/6-1 ENDOSCOPIC CLIPPING DEVICE, ENDOSCOPIC CLIPS received FDA 510(k) clearance under submission number K990687, sponsored by Olympus Optical, Co.. 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 1999-03-26.

Classification & Regulation

This clearance is catalogued under FDA product code PKL and 21 CFR 876.4400, within the Gastroenterology, Urology review panel as a Class II device.