meddevicedb.com FDA Device Reference

Disposable Grounding Pad

K231985 Class II Traditional
Decision Date
2024-02-16
Sponsor / Applicant
Shenzhen Mecun Medical Supply Co., Ltd.

Technical Specification

510(k) Submission ID K231985
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2024-02-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Grounding Pad received FDA 510(k) clearance under submission number K231985, sponsored by Shenzhen Mecun Medical Supply 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 2024-02-16.

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.