meddevicedb.com FDA Device Reference

Procedure mask/Surgical mask/Face mask

K223232 Class II Traditional
Decision Date
2023-03-06
Sponsor / Applicant
Winner Medical Co., Ltd.

Technical Specification

510(k) Submission ID K223232
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2023-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Procedure mask/Surgical mask/Face mask received FDA 510(k) clearance under submission number K223232, sponsored by Winner Medical 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 2023-03-06.

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.