meddevicedb.com FDA Device Reference

AIRLIFE HEATED VENTILATOR AND BREATHING CIRCUITS

K993833 Class II Special
Decision Date
1999-12-10
Sponsor / Applicant
Allegiance Healthcare Corp.

Technical Specification

510(k) Submission ID K993833
Product Code BZE
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5270
Decision Date 1999-12-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AIRLIFE HEATED VENTILATOR AND BREATHING CIRCUITS received FDA 510(k) clearance under submission number K993833, sponsored by Allegiance Healthcare Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1999-12-10.

Classification & Regulation

This clearance is catalogued under FDA product code BZE and 21 CFR 868.5270, within the Anesthesiology review panel as a Class II device.