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ELECTROSURGICAL GROUND PAD-DISPERSIVE

K830613 Class II Traditional
Decision Date
1983-04-12
Sponsor / Applicant
Con Med Equipment, Inc.

Technical Specification

510(k) Submission ID K830613
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1983-04-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTROSURGICAL GROUND PAD-DISPERSIVE received FDA 510(k) clearance under submission number K830613, sponsored by Con Med Equipment, 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 1983-04-12.

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.