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FAS-CLEAN ELECTROSURGICAL COATED ACTIVE BLADE

K073616 Class II Traditional
Decision Date
2008-07-23
Sponsor / Applicant
Electromedics Co. , Ltd.

Technical Specification

510(k) Submission ID K073616
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2008-07-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FAS-CLEAN ELECTROSURGICAL COATED ACTIVE BLADE received FDA 510(k) clearance under submission number K073616, sponsored by Electromedics 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 2008-07-23.

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.