meddevicedb.com FDA Device Reference

Surgical face mask

K211296 Class II Traditional
Decision Date
2021-09-11
Sponsor / Applicant
Sunsmed Protective Products , Ltd.

Technical Specification

510(k) Submission ID K211296
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2021-09-11
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 K211296, sponsored by Sunsmed Protective Products , 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 2021-09-11.

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.