meddevicedb.com FDA Device Reference

Surgical Face Masks (Sterile), Surgical Face Masks (Non-sterile)

K202843 Class II Traditional
Decision Date
2021-01-12
Sponsor / Applicant
B.J.ZH.F.PANTHER MEDICAL EQUIPMENT CO., Ltd.

Technical Specification

510(k) Submission ID K202843
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2021-01-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Surgical Face Masks (Sterile), Surgical Face Masks (Non-sterile) received FDA 510(k) clearance under submission number K202843, sponsored by B.J.ZH.F.PANTHER MEDICAL EQUIPMENT 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 2021-01-12.

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.