meddevicedb.com FDA Device Reference

Medical Face Mask

K212994 Class II Traditional
Decision Date
2022-01-17
Sponsor / Applicant
Guangzhou Quantum Laser Intelligent Equipment Co., Ltd.

Technical Specification

510(k) Submission ID K212994
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2022-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Medical Face Mask received FDA 510(k) clearance under submission number K212994, sponsored by Guangzhou Quantum Laser Intelligent Equipment 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 2022-01-17.

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.