meddevicedb.com FDA Device Reference

EC50 TOXCO+ BREATH CARBON MONOXIDE MONITOR

K070259 Class II Traditional
Decision Date
2008-02-21
Sponsor / Applicant
Bedfont Scientific, Ltd.

Technical Specification

510(k) Submission ID K070259
Product Code CCJ
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1430
Decision Date 2008-02-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EC50 TOXCO+ BREATH CARBON MONOXIDE MONITOR received FDA 510(k) clearance under submission number K070259, sponsored by Bedfont Scientific, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2008-02-21.

Classification & Regulation

This clearance is catalogued under FDA product code CCJ and 21 CFR 868.1430, within the Anesthesiology review panel as a Class II device.