meddevicedb.com FDA Device Reference

ADDITIONAL ELECTROSURGICAL GROUND PADS

K885172 Class II Traditional
Decision Date
1989-01-06
Sponsor / Applicant
Conmedcorp

Technical Specification

510(k) Submission ID K885172
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1989-01-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADDITIONAL ELECTROSURGICAL GROUND PADS received FDA 510(k) clearance under submission number K885172, sponsored by Conmedcorp. 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 1989-01-06.

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.