meddevicedb.com FDA Device Reference

TOTAL O2

K013472 Class II Traditional
Decision Date
2001-11-28
Sponsor / Applicant
Chad Therapeutics, Inc.

Technical Specification

510(k) Submission ID K013472
Product Code CAW
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5440
Decision Date 2001-11-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL O2 received FDA 510(k) clearance under submission number K013472, sponsored by Chad Therapeutics, 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 2001-11-28.

Classification & Regulation

This clearance is catalogued under FDA product code CAW and 21 CFR 868.5440, within the Anesthesiology review panel as a Class II device.