meddevicedb.com FDA Device Reference

UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES

K023767 Class II Special
Decision Date
2002-11-29
Sponsor / Applicant
The Olympus Optical Co.

Technical Specification

510(k) Submission ID K023767
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2002-11-29
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES received FDA 510(k) clearance under submission number K023767, sponsored by The Olympus Optical Co.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2002-11-29.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.