meddevicedb.com FDA Device Reference

HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE

K024138 Class II Traditional
Decision Date
2003-03-12
Sponsor / Applicant
Olympus Optical Co., Ltd.

Technical Specification

510(k) Submission ID K024138
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2003-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE received FDA 510(k) clearance under submission number K024138, sponsored by Olympus Optical Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2003-03-12.

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.