meddevicedb.com FDA Device Reference

C2 NASAL MASK

K033759 Class II Traditional
Decision Date
2004-02-19
Sponsor / Applicant
Respironics, Inc.

Technical Specification

510(k) Submission ID K033759
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2004-02-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

C2 NASAL MASK received FDA 510(k) clearance under submission number K033759, sponsored by Respironics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2004-02-19.

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.