meddevicedb.com FDA Device Reference

3 Layer Surgical Mask (134252531)

K231618 Class II Traditional
Decision Date
2023-07-28
Sponsor / Applicant
Original Mattress Factory, Inc.

Technical Specification

510(k) Submission ID K231618
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2023-07-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3 Layer Surgical Mask (134252531) received FDA 510(k) clearance under submission number K231618, sponsored by Original Mattress Factory, Inc.. 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 2023-07-28.

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.