meddevicedb.com FDA Device Reference

Comfort Guard Mask, level 1, Comfort Guard Mask, level 3

K210860 Class II Traditional
Decision Date
2022-04-07
Sponsor / Applicant
Gri-Alleset, Inc.

Technical Specification

510(k) Submission ID K210860
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2022-04-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Comfort Guard Mask, level 1, Comfort Guard Mask, level 3 received FDA 510(k) clearance under submission number K210860, sponsored by Gri-Alleset, 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 2022-04-07.

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.