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THE INCOURAGE SYSTEM

K051383 Class II Traditional
Decision Date
2005-06-17
Sponsor / Applicant
Respiratory Technologies, Incorporated

Technical Specification

510(k) Submission ID K051383
Product Code BYI
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5665
Decision Date 2005-06-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE INCOURAGE SYSTEM received FDA 510(k) clearance under submission number K051383, sponsored by Respiratory Technologies, Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2005-06-17.

Classification & Regulation

This clearance is catalogued under FDA product code BYI and 21 CFR 868.5665, within the Anesthesiology review panel as a Class II device.