meddevicedb.com FDA Device Reference

AirLife™ Open Et Oxygen Mask, AirLife™ Open Et+ Oxygen Mask

K230915 Class II Traditional
Decision Date
2024-11-12
Sponsor / Applicant
Vyaire Medical, Inc.

Technical Specification

510(k) Submission ID K230915
Product Code CCK
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1400
Decision Date 2024-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AirLife™ Open Et Oxygen Mask, AirLife™ Open Et+ Oxygen Mask received FDA 510(k) clearance under submission number K230915, sponsored by Vyaire Medical, 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 2024-11-12.

Classification & Regulation

This clearance is catalogued under FDA product code CCK and 21 CFR 868.1400, within the Anesthesiology review panel as a Class II device.