meddevicedb.com FDA Device Reference

CO TEST

K843845 Class II Traditional
Decision Date
1984-10-12
Sponsor / Applicant
Erich Jaeger, Inc.

Technical Specification

510(k) Submission ID K843845
Product Code CCJ
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1430
Decision Date 1984-10-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CO TEST received FDA 510(k) clearance under submission number K843845, sponsored by Erich Jaeger, 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 1984-10-12.

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.