meddevicedb.com FDA Device Reference

Surgical Face Mask

K200847 Class II Traditional
Decision Date
2020-04-23
Sponsor / Applicant
Mexpo International, Inc.

Technical Specification

510(k) Submission ID K200847
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2020-04-23
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 K200847, sponsored by Mexpo International, Inc.. 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 2020-04-23.

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.