meddevicedb.com FDA Device Reference

Face Mask

K210007 Class II Traditional
Decision Date
2021-04-23
Sponsor / Applicant
Jinhua Jingdi Medical Supplies Co., Ltd.

Technical Specification

510(k) Submission ID K210007
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2021-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Face Mask received FDA 510(k) clearance under submission number K210007, sponsored by Jinhua Jingdi Medical Supplies 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 2021-04-23.

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.