meddevicedb.com FDA Device Reference

PROTECTION PLUS EARLOOP PROCEDURE MASK

K042654 Class II Traditional
Decision Date
2004-12-17
Sponsor / Applicant
Safety-Med Products, Inc.

Technical Specification

510(k) Submission ID K042654
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2004-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROTECTION PLUS EARLOOP PROCEDURE MASK received FDA 510(k) clearance under submission number K042654, sponsored by Safety-Med Products, 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 2004-12-17.

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.