meddevicedb.com FDA Device Reference

Yadu Medical Face Mask (Level 1)

K212330 Class II Traditional
Decision Date
2022-03-14
Sponsor / Applicant
Henan Yadu Industrial Co., Ltd.

Technical Specification

510(k) Submission ID K212330
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2022-03-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Yadu Medical Face Mask (Level 1) received FDA 510(k) clearance under submission number K212330, sponsored by Henan Yadu Industrial 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 2022-03-14.

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.