meddevicedb.com FDA Device Reference

CONWAY STUART MEDICAL MODEL C4 ELECTROSURGICAL GENERATOR

K983986 Class II Traditional
Decision Date
1999-03-23
Sponsor / Applicant
Conway Stuart Medical, Inc.

Technical Specification

510(k) Submission ID K983986
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1999-03-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONWAY STUART MEDICAL MODEL C4 ELECTROSURGICAL GENERATOR received FDA 510(k) clearance under submission number K983986, sponsored by Conway Stuart Medical, 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 1999-03-23.

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.