meddevicedb.com FDA Device Reference

LAPARO-THORACO VIDEOSCOPE XLTF-VAW

K053382 Class II Traditional
Decision Date
2006-05-26
Sponsor / Applicant
Olympus Medical Systems Corporation

Technical Specification

510(k) Submission ID K053382
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2006-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LAPARO-THORACO VIDEOSCOPE XLTF-VAW received FDA 510(k) clearance under submission number K053382, sponsored by Olympus Medical Systems Corporation. 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 2006-05-26.

Classification & Regulation

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