meddevicedb.com FDA Device Reference

PERFORMAX TOTAL FACE MASK

K072592 Class II Traditional
Decision Date
2007-12-19
Sponsor / Applicant
Respironics Inc., Sleep & Home Respiratory Group

Technical Specification

510(k) Submission ID K072592
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2007-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERFORMAX TOTAL FACE MASK received FDA 510(k) clearance under submission number K072592, 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 2007-12-19.

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.