meddevicedb.com FDA Device Reference

Medical Surgical Mask

K202029 Class II Traditional
Decision Date
2020-12-16
Sponsor / Applicant
Beijing Biosis Healing Biolog Ical Technology Co., Ltd.

Technical Specification

510(k) Submission ID K202029
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2020-12-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Medical Surgical Mask received FDA 510(k) clearance under submission number K202029, sponsored by Beijing Biosis Healing Biolog Ical Technology 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 2020-12-16.

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.