meddevicedb.com FDA Device Reference

Topwide Surgical Face Mask

K210102 Class II Traditional
Decision Date
2021-12-17
Sponsor / Applicant
Topwide (Hubei) Medical Products Manufacturer

Technical Specification

510(k) Submission ID K210102
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2021-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Topwide Surgical Face Mask received FDA 510(k) clearance under submission number K210102, sponsored by Topwide (Hubei) Medical Products Manufacturer. 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 2021-12-17.

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.