meddevicedb.com FDA Device Reference

Disposable Medical Face Mask

K202676 Class II Traditional
Decision Date
2021-11-05
Sponsor / Applicant
Zhejiang Senhong Medical&Instrument Co., Ltd.

Technical Specification

510(k) Submission ID K202676
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2021-11-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Medical Face Mask received FDA 510(k) clearance under submission number K202676, sponsored by Zhejiang Senhong Medical&Instrument 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 2021-11-05.

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.