meddevicedb.com FDA Device Reference

COMFORTGEL FULL FACE MASK

K073600 Class II Traditional
Decision Date
2008-04-25
Sponsor / Applicant
Respironics Inc., Sleep & Home Respiratory Group

Technical Specification

510(k) Submission ID K073600
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2008-04-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMFORTGEL FULL FACE MASK received FDA 510(k) clearance under submission number K073600, sponsored by Respironics Inc., Sleep & Home Respiratory Group. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2008-04-25.

Classification & Regulation

This clearance is catalogued under FDA product code BZD and 21 CFR 868.5905, within the Anesthesiology review panel as a Class II device.