meddevicedb.com FDA Device Reference

3 Ply Medical Grade Single Use Procedural Disposable Face Mask

K220637 Class II Traditional
Decision Date
2022-03-25
Sponsor / Applicant
Kdi Med Supply

Technical Specification

510(k) Submission ID K220637
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2022-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3 Ply Medical Grade Single Use Procedural Disposable Face Mask received FDA 510(k) clearance under submission number K220637, sponsored by Kdi Med Supply. 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 2022-03-25.

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.