meddevicedb.com FDA Device Reference

KP Protective Face Mask

K243342 Class II Traditional
Decision Date
2025-12-22
Sponsor / Applicant
Kp Trading Co., Ltd.

Technical Specification

510(k) Submission ID K243342
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2025-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KP Protective Face Mask received FDA 510(k) clearance under submission number K243342, sponsored by Kp Trading 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 2025-12-22.

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.