meddevicedb.com FDA Device Reference

NON-STERILE SURGICAL MASK

K051291 Class II Traditional
Decision Date
2005-09-20
Sponsor / Applicant
A.R. Medicom, Inc.

Technical Specification

510(k) Submission ID K051291
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2005-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NON-STERILE SURGICAL MASK received FDA 510(k) clearance under submission number K051291, sponsored by A.R. Medicom, 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 2005-09-20.

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.