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REPROCESSED ELECTROSURGICAL ELECTRODES

K012669 Class II Traditional
Decision Date
2002-06-27
Sponsor / Applicant
Surgical Instruments Service and Savings, Inc.

Technical Specification

510(k) Submission ID K012669
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2002-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REPROCESSED ELECTROSURGICAL ELECTRODES received FDA 510(k) clearance under submission number K012669, sponsored by Surgical Instruments Service and Savings, Inc.. 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 2002-06-27.

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.