meddevicedb.com FDA Device Reference

Medical Protective Mask (model: 8862, 8862A, 8862B, 8862C, 8862D, 8862E)

K223068 Class II Traditional
Decision Date
2022-11-23
Sponsor / Applicant
Guangdong Golden Leaves Technology Development Co., Ltd.

Technical Specification

510(k) Submission ID K223068
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2022-11-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Medical Protective Mask (model: 8862, 8862A, 8862B, 8862C, 8862D, 8862E) received FDA 510(k) clearance under submission number K223068, sponsored by Guangdong Golden Leaves Technology Development 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 2022-11-23.

Classification & Regulation

This clearance is catalogued under FDA product code FXX and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.