meddevicedb.com FDA Device Reference

Surgical Face Mask

K182514 Class II Traditional
Decision Date
2019-01-24
Sponsor / Applicant
Xiantao Zhibo Non-Woven Products Co., Ltd.

Technical Specification

510(k) Submission ID K182514
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2019-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Surgical Face Mask received FDA 510(k) clearance under submission number K182514, sponsored by Xiantao Zhibo Non-Woven Products 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 2019-01-24.

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.